Tag | Content |
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EnhancerAtlas ID | HS095-07845 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:113275790-113278120 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DMRT3 | MA0610.1 | chr12:113277140-113277151 | AATGTATCAAC | + | 6.02 | FOXP1 | MA0481.2 | chr12:113277377-113277389 | GAGTAAACAGAA | + | 6.27 | ZNF263 | MA0528.1 | chr12:113276377-113276398 | GGGGGAGAAGAAGAAAGAAAA | + | 6.17 | ZNF263 | MA0528.1 | chr12:113276371-113276392 | AAGGGAGGGGGAGAAGAAGAA | + | 6.42 | ZNF263 | MA0528.1 | chr12:113276367-113276388 | GGGGAAGGGAGGGGGAGAAGA | + | 6.72 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH12I112839 | chr12 | 113275681 | 113275830 | GH12I112838 | chr12 | 113276419 | 113278189 |
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Enhancer Sequence | GACACAGTTA GCCAAGTATA AAGATATGTC TAGTGGAGTC TACAAACAAA TAAAGGGCCA 60 GTCACCAACA AATACACTCT AGTATGTGCA GAGCTATAAT CATAGAATCA GAGTGAACTG 120 TGGAGCACAA AGACAGTCAC CTAGCTCAGA CCTGAGGGTG ATGATGGAGA GCTTCCTGGA 180 AGAAGTGATG TGTAAGCTGA GACCAGGAGA GGGAGGAGCA CTACGTGGAG GAGACAGAGG 240 AGTTCCCAGT GGGGGACACG GCATCTGCCA AGCCCAACTG TGAGAGAGAA CATGGGATTT 300 TATAAGAACA GAATGGAATT CAGTCTGGCT AAAAAGATTA ACAGGACCCC CAGGTCCCGT 360 TGGCATTCTG AGGATGTGGG GGACCCACAG CATCCCTTCT GCACTCCCAT TAGTCTGGTT 420 GGGGTAAATT TCATCCAAAG GGGCCTTTAT ACCAGCTGGG CATGGGCAAA AGGTTCTGTG 480 GTGTGGCTGC CCCTCCTTTT CTTCAGGATT CATTAAAATC CCATTCACTG TGCTATAAAG 540 AGACTTCCTG CAGACACCTG CCCATGTTGG CATCCAAGGG GAAGGGAGGG GGAGAAGAAG 600 AAAGAAAAGA AAAAGGATTA ATTTTCTGCA CACCTCTGCT GTTGAATGCT TCAGAGCCTT 660 CATGCCCCGA CAGCATTTCC ATCATCCCAC TCCTTTAGGG AGTTATAATT TATTAATAGA 720 GACATCTGGC GAGTATTTAT TATGTGACTG TTGTGTGCAT GCAATGAAGA ATCAAGGTGG 780 GAGGCAGGAA AGATATGGAA GGCTGTCCTT TGCCTTCCAT TTTGCCCTGT TTGTATTTCA 840 GGGGGAAACA TCTATGAGGG CTTCTACCTG GAGTCTGGGC TAATTTCCTT TTGTCTCGGG 900 GTCCACCAAT GCTGGCCTTG GTGGGTGGCT TCATTCTGAC CCCTCATGGT GCACCAGAGC 960 AGGTGCCTTC AGGTAGCAGA TGAAGCACAT TGAGAAGGCC GGGGCCGGTT TCTCAAGTCC 1020 TGGACCATCC TCTCTCCAGT CATGATTCTT GGCAATTCCC TTTCTCCTTG TGAGTCTCAG 1080 GCATCTGGGA AAATGAGCAG GTTACCACAG TGGTCTTTAG ACTTTTTCTT ACCAGTGAAA 1140 GTCTTTCTTT GAATAATACT TTATTCAGAA GCTAAATCTT TGAGGCAGAT AAGAGTGGAG 1200 CTGGATAAAG ACCTTTAGTG GCTGAAAGCA TTAAAAATAT CATGGTAAAC ATTATACAAC 1260 TGGAATTTAA CATAATGCTA AACTGTAAAA TAAGGGTAGG AAGTCTAACA AGTTTCACTC 1320 TTTTTTTTCT TTTTTTTTGC CATGGTGAAT AATGTATCAA CTTTCGCTGT GTAACAAACC 1380 ATCTTAAAAC TCAGTGACTT AGAACAGTTA CTTGTTCTCA GGGATCTGGG CTTGGTGAGT 1440 GGCTCTGTGG ACTTTGGCTA GGCTCATTTA TGCATCAAAG GGTTGGCTGA TCTAAGATGC 1500 CAGTGGCTGG AATGATACAT TCTTTTCCAC ATGCCTCACC TTCCAACAGG ATATCCTGGG 1560 TTTTCTCATG GTGATGACAG GGTATAAGAG TAAACAGAAA CACACAAGGC CTTTGGAGGC 1620 ATTGCCTCTG GACTAGTGCA ACATCACTCC CCTGCATTTT ATTTCCCACA GCAAGTCCTA 1680 AGTCTTGGCT AGATTTAAGG AGTAGGAAAA TAGACTCTAG AGCCAGACGT GGTGGCTCAT 1740 GCCCAGAATC CCAGCACTTT GGGAGGCCGA GATAGGCAGA GAGCCTGAGG TCAGGAATTC 1800 GAGACCAGCC TGGCCAACAT GGTGAAATCC TGTCTCTACT GAAAATACAA AACACTATCT 1860 GGGTGTGGTG GTGCATGCCT GTAGTCCCAG CTACTCAGGA GGCTGACACA GGAGAATTGC 1920 TTGAACCCAG GAGGTGGAGG TTGCGGTGAG CCAAGACTGT GCCACTGCAC TCCAGCCTGG 1980 GCAACCGAGT GAGACACCAT CTCAAAAAAA AAGAAAAGAA AAGAAGATAG ACCCTGACTC 2040 TTTGGTGATC AATTTCAAAT TCACATGGCA TAGGGCATGG ATACAGAGAA GAGTGAAATA 2100 TTAGGGACAT CCTTATAATA AACCATATTT CATGCTTTTA CTAAAATATT AAATATTAAT 2160 TTTTTCCCCA ATGTTTGTCG CTTTTTTTCT TTCTAAATTT TTAAATTTTT TTGACATAAA 2220 ATAGTTTACA TATTTTTGGG GTACATGTGA TATTTTGGTA CCTATATACA ATGTGGAATA 2280 ATCAAATCAG GGTAATAGAA ATACGCATCA CCTCAAACAT TTATCATTTA 2330
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