Chrom Start End Enhancer ID Tissues that enhancer appears More
chr11 563885 571395 enh1603

Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr11 560880 rs568946500 G A 1787334
chr11 560889 rs538075413 C T 1787335
chr11 560906 rs548282179 T G 1787336
chr11 560910 rs568133789 G A 1787337
chr11 560936 rs533888299 G C 1787338
chr11 560954 rs553760535 G A 1787339
chr11 560975 rs538961426 G C,T 1787340
chr11 560977 rs542208050 T G 1787341
chr11 560982 rs575733502 G A 1787342
chr11 561014 rs544432445 C T 1787343
chr11 561026 rs183456713 G A 1787344
chr11 561053 rs532577773 C G 1787345
chr11 561060 rs530708929 TGGGAGCGCG T 1787346
chr11 561068 rs146684367 C T 1787347
chr11 561256 rs531530166 G A 1787348
chr11 561476 rs142735008 AG A 1787349
chr11 561504 rs7928340 T C 1787350
chr11 561600 rs575869678 G C 1787351
chr11 561654 rs574697317 G A,T 1787352
chr11 561673 rs138740611 C T 1787353
chr11 561703 rs114913728 G A,C 1787354
chr11 561787 rs200646397 G A,T 1787355
chr11 561798 rs143459467 G A 1787356
chr11 561957 rs116653071 T C 1787357
chr11 561970 rs58334317 C A 1787358
chr11 562029 rs12575035 T C 1787359
chr11 562059 rs556472525 C T 1787360
chr11 562065 rs141809126 C T 1787361
chr11 562154 rs146160844 T C 1787362
chr11 562159 rs371463729 G A 1787363
chr11 562219 rs2242183 C G 1787364
chr11 562421 rs2242182 G A,C 1787365
chr11 562424 rs528974630 G C 1787366
chr11 562437 rs11246189 G A 1787367
chr11 562451 rs560509320 C G 1787368
chr11 562492 rs571014012 C T 1787369
chr11 562570 rs535970268 C T 1787370
chr11 562571 rs182995401 G A,T 1787371
chr11 562582 rs572478121 C T 1787372
chr11 562707 rs111862990 G C 1787373
chr11 562820 rs111838516 T C 1787374
chr11 562844 rs533702049 G A 1787375
chr11 562934 rs566058290 T C 1787376
chr11 562935 rs533144681 G C 1787377
chr11 562953 rs558151510 G A 1787378
chr11 563056 rs369430668 CCT C 1787379
chr11 563072 rs141755107 C G,T 1787380
chr11 563101 rs184226611 G A,C 1787381
chr11 563128 rs146232317 C T 1787382
chr11 563148 rs552683879 G C 1787383
chr11 563149 rs201373170 C T 1787384
chr11 563257 rs34954482 G A,C 1787385
chr11 563271 rs35670527 C A,T 1787386
chr11 563289 rs34358040 G A 1787387
chr11 563303 rs139808560 C T 1787388
chr11 563364 rs199789820 G A 1787389
chr11 563400 rs34822421 C T 1787390
chr11 563412 rs140192306 C T 1787391
chr11 563489 rs201007942 G A,C 1787392
chr11 563571 rs371569281 G A 1787393
chr11 563649 rs7109278 C T 1787394
chr11 563798 rs73399078 G A,C 1787395
chr11 563888 rs181071400 T C 1787396
chr11 564045 rs1599727 T C 1787397
chr11 564110 rs568948679 C T 1787398
chr11 564263 rs368368198 T C 1787399
chr11 564268 rs1016474 G A,C 1787400
chr11 564295 rs1599726 A G 1787401
chr11 564345 rs368088496 C T 1787402
chr11 564366 rs371210174 AC A 1787403
chr11 564501 rs190638077 C T 1787404
chr11 564503 rs181795310 T C 1787405
chr11 564504 rs114656478 C A,G 1787406

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
chr11 554855 560779 - C11orf35 ENSG00000185522.4 560779 0.8 1.0 97 10360
chr11 560404 564021 + RASSF7 ENSG00000099849.10 560404 0.77 1.0 472 10361


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
chr11 568150 568171 - hsa-miR-210-5p MIMAT0026475 568416 0.809941 0.676023 3805 196