EnhancerDB
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Chromosome characteristics of ZNF274[chr13:111212092-111218494]
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Enhancers possibly regulated by ZNF274[chr13:111212092-111218494]
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Chrom Start End Enhancer ID Tissues that enhancer appears More
chr13 111186805 111212195 enh15501
Prostate (PC-3) Liver (HepG2) Epithelial (MCF-7) Cervix (HeLa-S3) Brain (SK-N-SH) Esophagus Astrocyte Bone (Osteoblast) Stomach Placenta Colon (HCT116) Thyroid Peripheral Blood (MM.1S) Pancreas (Panc1) Lung (PC-9) Pancreas Spleen Neural Stem Cells (H9) Heart
chr13 111212014 111212166 vista17066
VISTA
chr13 111212967 111213224 vista17067
VISTA
SNP sites on ZNF274[chr13:111212092-111218494]
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Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr13 111212152 rs145007285 G C 3396072
chr13 111212272 rs560214176 C A 3396073
chr13 111212304 rs531681994 A C 3396074
chr13 111212582 rs115989143 G A,C 3396075
chr13 111212621 rs570012034 T C 3396076
chr13 111212771 rs140416382 G A 3396077
chr13 111212971 rs186100863 A G 3396078
chr13 111213050 rs142098260 G C 3396079
chr13 111213087 rs181264258 A G 3396080
chr13 111213118 rs11425407 C CA 3396081
chr13 111213131 rs9805796 T C 3396082
chr13 111213209 rs378859 C A 3396083
chr13 111213217 rs395865 T C 3396084
chr13 111213352 rs567956471 G A 3396085
chr13 111213445 rs569532868 A C 3396086
chr13 111213466 rs4506764 A G 3396087
chr13 111213493 rs2893368 G A 3396088
chr13 111213500 rs539579616 C T 3396089
chr13 111213582 rs13313297 T C 3396090
chr13 111213591 rs13313269 G A 3396091
chr13 111213600 rs573919517 A G 3396092
chr13 111213680 rs111681301 C G 3396093
chr13 111213926 rs567857501 G T 3396094
chr13 111213945 rs528805994 G A 3396095
chr13 111213964 rs565647034 C T 3396096
chr13 111213964 rs576644241 CG C 3396097
chr13 111214102 rs565124650 GGCCTC G 3396098
chr13 111214111 rs559054985 T TCGCCC 3396099
chr13 111214111 rs80155236 T C 3396100
chr13 111214124 rs569393144 G GCCCCCCC 3396101
chr13 111214152 rs552869978 G C 3396102
chr13 111214286 rs73623121 C G 3396103
chr13 111214334 rs561560069 T C,G 3396104
chr13 111214541 rs73623124 C A,T 3396105
chr13 111214591 rs115391724 G A 3396106
chr13 111214665 rs555256268 A G 3396107
chr13 111214718 rs537922093 A G 3396108
chr13 111214729 rs538922573 CT C 3396109
chr13 111214733 rs552806079 T C 3396110
chr13 111214921 rs424904 G A 3396111
chr13 111214922 rs552542792 ACACGGGGTTTCAC A 3396112
chr13 111214937 rs190548052 A C 3396113
chr13 111214962 rs395289 C G 3396114
chr13 111215023 rs540840978 C T 3396115
chr13 111215047 rs77836417 A G 3396116
chr13 111215102 rs149967940 T C 3396117
chr13 111215291 rs555078721 G A 3396118
chr13 111215341 rs116714347 G C 3396119
chr13 111215356 rs113252033 GACCTTCTGGGGCGTGGAAAGCGC G 3396120
chr13 111215356 rs376885756 GACCTTCTGGGGCGTGGAAAGCGC G 3396121
chr13 111215379 rs549016251 C G 3396122
chr13 111215458 rs183108903 A G 3396123
chr13 111215513 rs2479435 C A 3396124
chr13 111215536 rs539796935 C T 3396125
chr13 111215537 rs67721460 T A 3396126
chr13 111215560 rs370135291 A G 3396127
chr13 111215562 rs146515940 G A 3396128
chr13 111215607 rs577596986 A T 3396129
chr13 111215713 rs563042779 G A 3396130
chr13 111215739 rs373023466 T C 3396131
chr13 111215764 rs376881932 G A 3396132
chr13 111215814 rs192320435 C T 3396133
chr13 111215843 rs140539134 C A,G 3396134
chr13 111215845 rs182350250 G T 3396135
chr13 111215850 rs9521843 G A 3396136
chr13 111215883 rs550807109 A G 3396137
chr13 111215916 rs569068841 G C 3396138
chr13 111215931 rs536643727 C G,T 3396139
chr13 111216019 rs76432504 A G 3396140
chr13 111216073 rs77443224 C G 3396141
chr13 111216422 rs143589317 CCT C 3396142
chr13 111216569 rs118035477 A G 3396143
chr13 111216844 rs111949680 C CCA,CCACA 3396144
chr13 111216844 rs397770354 C CCA 3396145
chr13 111216902 rs420176 G C 3396146
chr13 111216988 rs540666688 T G 3396147
chr13 111217025 rs392473 A T 3396148
chr13 111217053 rs60925888 A C,G 3396149
chr13 111217097 rs114306525 G A 3396150
chr13 111217188 rs143268340 A T 3396151
chr13 111217206 rs187099392 G T 3396152
chr13 111217243 rs766975 G A 3396153
chr13 111217422 rs766974 A G 3396154
chr13 111217437 rs560467779 C T 3396155
chr13 111217666 rs77941574 G T 3396156
chr13 111217760 rs562797292 AAAACT A 3396157
chr13 111217860 rs147544033 G A 3396158
chr13 111217913 rs454582 G T 3396159
chr13 111217948 rs74350032 C T 3396160
chr13 111218169 rs574500643 T C 3396161
chr13 111218216 rs445740 T C 3396162
chr13 111218218 rs572209035 G A 3396163
chr13 111218317 rs138531993 C T 3396164
chr13 111218396 rs540825410 C T 3396165
Genes possibly regulated by ZNF274[chr13:111212092-111218494]
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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
chr13 111175417 111214080 - RAB20 ENSG00000139832.3 111214080 0.75 1.0 1988 13021
Expression level of Genes
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miRNAs possibly regulated by ZNF274[chr13:111212092-111218494]
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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