EnhancerDB
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Chromosome characteristics of TCF7L2[chr16:85638253-85645854]
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Enhancers possibly regulated by TCF7L2[chr16:85638253-85645854]
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Chrom Start End Enhancer ID Tissues that enhancer appears More
chr16 85640485 85664563 enh16874
Bone Marrow (K562) Skin (Keratinocyte) Prostate (PC-3) Liver (HepG2) Epithelial (MCF-7) Brain (SK-N-SH) Large Intestine Liver Stomach Muscle (A673) Placenta Embryonic Stem Cell Line (H1-hESC) Pancreas Muscle (Myotube) Uterus Blood (T-cell) Heart
chr16 85631618 85639631 enh16873
Brain (SK-N-SH) Placenta Colon (HCT116) Pancreas Heart Stomach
SNP sites on TCF7L2[chr16:85638253-85645854]
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Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr16 85638258 rs55927086 G A 4626180
chr16 85638303 rs577690383 A G 4626181
chr16 85638315 rs553737665 C T 4626182
chr16 85638509 rs190568838 C T 4626183
chr16 85638520 rs562813173 T G 4626184
chr16 85638568 rs181790840 C T 4626185
chr16 85638598 rs186219025 T A 4626186
chr16 85638609 rs139272259 G A 4626187
chr16 85638613 rs141720622 T C 4626188
chr16 85638614 rs566532704 G A 4626189
chr16 85638624 rs369091263 C T 4626190
chr16 85638625 rs188584645 G A 4626191
chr16 85638627 rs569234629 G T 4626192
chr16 85638634 rs538125364 A G 4626193
chr16 85638771 rs553632061 G A 4626194
chr16 85638799 rs116475272 C G 4626195
chr16 85639014 rs79557046 G A 4626196
chr16 85639068 rs75179386 G A,T 4626197
chr16 85639228 rs181338241 C T 4626198
chr16 85639393 rs150938367 G T 4626199
chr16 85639397 rs149457891 G A,T 4626200
chr16 85639407 rs74031881 G A,T 4626201
chr16 85639450 rs143905417 C A 4626202
chr16 85639475 rs148190348 C A,T 4626203
chr16 85639650 rs527965598 G A 4626204
chr16 85639726 rs74031882 C T 4626205
chr16 85639763 rs187381627 C T 4626206
chr16 85639764 rs534567797 G A 4626207
chr16 85639778 rs574245079 T C 4626208
chr16 85639837 rs11866745 C A 4626209
chr16 85639897 rs550700608 CATGT C 4626210
chr16 85639902 rs545102316 G C 4626211
chr16 85639918 rs113344091 G T 4626212
chr16 85640028 rs139330160 C A,G 4626213
chr16 85640046 rs144079800 C G 4626214
chr16 85640125 rs183604393 G A 4626215
chr16 85640209 rs58534183 C G,T 4626216
chr16 85640311 rs76618142 G A 4626217
chr16 85640424 rs576482738 G T 4626218
chr16 85640451 rs77535849 C T 4626219
chr16 85640490 rs561609996 G A 4626220
chr16 85640493 rs571490818 C G,T 4626221
chr16 85640524 rs187475409 G A 4626222
chr16 85640532 rs139597923 C T 4626223
chr16 85640535 rs116534600 G A 4626224
chr16 85640570 rs546297352 T TTC 4626225
chr16 85640671 rs555152871 T TGG 4626226
chr16 85640671 rs559179790 T G 4626227
chr16 85640986 rs539897080 G A,T 4626228
chr16 85641112 rs554972910 A C 4626229
chr16 85641136 rs575225368 A G 4626230
chr16 85641154 rs577413862 C T 4626231
chr16 85641212 rs145216627 C T 4626232
chr16 85641303 rs150781540 AG A 4626233
chr16 85641323 rs547804915 C T 4626234
chr16 85641566 rs75804642 C T 4626235
chr16 85641592 rs74031885 C A 4626236
chr16 85641606 rs201952125 C A,G,T 4626237
chr16 85641608 rs190563521 C A 4626238
chr16 85641687 rs541484145 G A 4626239
chr16 85641819 rs3935120 C A,T 4626240
chr16 85641897 rs546787193 C A,T 4626241
chr16 85642043 rs3935121 T C 4626242
chr16 85642099 rs78527985 G A 4626243
chr16 85642124 rs113661090 T G 4626244
chr16 85642129 rs7195360 C G 4626245
chr16 85642135 rs148138741 G A 4626246
chr16 85642220 rs533265086 G A 4626247
chr16 85642226 rs189124304 A G 4626248
chr16 85642246 rs79074971 T C 4626249
chr16 85642370 rs572761137 CTT C 4626250
chr16 85642405 rs150266364 T C 4626251
chr16 85642475 rs78323107 C T 4626252
chr16 85642705 rs116622422 G A 4626253
chr16 85642747 rs74031886 G A 4626254
chr16 85642759 rs551838250 C G 4626255
chr16 85642820 rs550750823 C T 4626256
chr16 85642822 rs117004110 G A 4626257
chr16 85642857 rs59085364 C A 4626258
chr16 85642888 rs115845196 A G 4626259
chr16 85643029 rs76385022 G T 4626260
chr16 85643078 rs74655905 G A 4626261
chr16 85643300 rs192203541 G A 4626262
chr16 85643328 rs533232947 T C 4626263
chr16 85643363 rs111976235 G T 4626264
chr16 85643573 rs577733649 T A,C 4626265
chr16 85643761 rs190510321 C G,T 4626266
chr16 85643786 rs142238912 G A 4626267
chr16 85643794 rs111478582 C G 4626268
chr16 85643817 rs547530835 G A 4626269
chr16 85643969 rs562865098 A G 4626270
chr16 85643977 rs575036907 G A 4626271
chr16 85644042 rs183049939 T G 4626272
chr16 85644159 rs529770033 G A,C 4626273
chr16 85644174 rs186969294 A G 4626274
chr16 85644243 rs144577070 C T 4626275
chr16 85644299 rs530660751 TGCC T 4626276
chr16 85644527 rs556284993 A G 4626277
chr16 85644556 rs147903994 T C 4626278
chr16 85644631 rs74031887 G A,C 4626279
chr16 85644658 rs117774844 G C 4626280
chr16 85644681 rs74031888 G C,T 4626281
chr16 85644788 rs534024952 G A 4626282
chr16 85645035 rs375671352 T C 4626283
chr16 85645058 rs565657609 G C,T 4626284
chr16 85645089 rs534569279 C A,T 4626285
chr16 85645112 rs547989370 G A 4626286
chr16 85645157 rs538202481 C G,T 4626287
chr16 85645178 rs556658419 T C 4626288
chr16 85645220 rs576443915 C T 4626289
chr16 85645254 rs532900216 GC G 4626290
chr16 85645305 rs116818028 G A 4626291
chr16 85645387 rs541707063 G A,C 4626292
chr16 85645414 rs543635180 G A,T 4626293
chr16 85645448 rs563422904 C G 4626294
chr16 85645565 rs528790104 C CT 4626295
chr16 85645610 rs141694087 G A 4626296
chr16 85645704 rs192771698 A C 4626297
chr16 85645780 rs530768908 A C 4626298
chr16 85645847 rs537679893 GGGGGC G 4626299
Genes possibly regulated by TCF7L2[chr16:85638253-85645854]
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Details of Genes
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand Gene Name Ensembl ID TSS TSI of Normal tissues TSI of Cancer tissues Distance to TFBS id More
chr16 85645015 85709810 + GSE1 ENSG00000131149.13 85645015 0.76 1.0 839 15131
Expression level of Genes
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miRNAs possibly regulated by TCF7L2[chr16:85638253-85645854]
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Details of miRNAs
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End strand miRNA Name miRBase ID TSS TSI of Normal tissues TSI of Cancer tissues Distance to TFBS id More
Expression level of miRNAs
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No results