Tag | Content |
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EnhancerAtlas ID | HS053-08604 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr12:3034080-3035660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr12:3035595-3035606 | AGCTGTGATTT | - | 6.14 | IRF1 | MA0050.2 | chr12:3034852-3034873 | CAAAAGAAAGTGAAAGATATG | - | 6.58 |
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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: 1 | ID | Chromosome | Start | End |
GH12I002925 | chr12 | 3034567 | 3034766 |
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Enhancer Sequence | TGCCTGTAAT CCCAGCACTT TGGGAGGCCG ACACGGGCGG ATCACAAGGT CAGGAGATCA 60 AGACCATCCT GGCTAACACG GTGAAACCCT GTCTCTACTA AAAATTAGCC AGGTGTGGTG 120 GCGGGCGCCT GTAGTCCCAG CTACTCGGGA GGTTGAGGCA CGAGAATGGC GTGAACCCGG 180 GAGGCGGAGC TTGCAGTGAG CCGAGATCAC GCCACTACAC TCCAGCCTGG GCGACGGAGC 240 AAGACTCCGT CCGTCTCAAA AAAAAAAAGA GCAGTAAGAA CCTGTGAGGA ATTTTAAGCT 300 GAACAATGAT ATGATCACAG TTGAGCTGTG GAAAAATTAC TGTGTACCAG AAAGAAGGAA 360 TTGAAGGGGG AAGTCCAGAA ACAGGAAAGC TATTTAGGAG ATCGTTTGAC TGATGATGGC 420 CTGACCTCCA GTTCCAATAT AGTGTGGTGT TTGCAAAAGC ACAGGCAGGG GAGATGCAGA 480 ATTGCTCTGC TAGGGCAATG AGAAGAGACA AGAGAGGTAC CAGGAGGAAG GGAGGGGGTG 540 ATTCCGCTGA ACAAAGAAGG ATGTGTGTCT GCCTACGTGC TAGGGGAGCA GGGAAGTAGC 600 TGGAGCCTGA CATTGTGAGT GTCCATCATG TGTCAGGCAC TTGACATGTA CTACCTCATC 660 TGATTTAATA GTTGTAATAG TGCCTTGGGG GTTTGTAAAG ACAGTTTTCC TGTCTTTAAC 720 ATGAAGGTGA CCATGGTACT TTCCTATTAT TTTACTACCA CTATTTTTAC AACAAAAGAA 780 AGTGAAAGAT ATGCGTTGGA CAGATAGGAT GAGTCGGAGC AAAAATAATT TTCTATTTAA 840 CCAAAGCTAA ATTACTCACC CTGAGTCAAC TAGCTGAAAA GTGGCAGATT TAGATTTTCT 900 GATTCTTAGT CTGGTTCTTT ATCCCTGACT GTAAACACCA CACTGTCTCC TTGTGCACTG 960 CTCTATGAAA TGGCTGTTCG TTTTCAGAAT TGGCCTTCCA GTGCCAGGTG AGTTAACGCC 1020 TTTTCATGTC TCAACAGGTT GCATCTTGAC TATAAAACCC ATTAAGTGCT GTTTTGATTA 1080 AATTCTAAGA AGTGTCAGTT TGGCAGATTA TGTCCCTGTA AGTGGGTCCA ATTTGCTTGT 1140 CTTAAAAGTT TCAGAGAGAT CTTTGATCTC TCAAGACAGA TTCACGGGAA CTGAGTTCTT 1200 GGTATTAAAA TGGCATTTGA AAGCATAGTA ATAGGTGAAG ATAGCCATAC GATAGTGATA 1260 TCTCAGGAGT TTCTGCCTTT CTGCTACCAA TAAAAAGGGG GGGTGCCAGG TGTGGTGGCT 1320 CATGCCTGTA ATCCCAGCAC TTTGGGAAGC CGAGGTGGGC GGATCGCTTG AGCCCAGGAG 1380 TTTGAGATCA GTCTGGGCAA CTTGGTGAAA CCCCATCTCT ACAAAAAAAT TACCTGGACA 1440 TGGTGTAGTC CTATGTACTC AGGAGGCTGA GGTGGGAGGA TCACTTGAGC CCGGGAAGTT 1500 GAGGCTGCAC TGAGCAGCTG TGATTTGGCC ACTGCACTCC CACCTGGGCA ACAGAGTGAA 1560 ACCCTGTCTC AAAAAATAAT 1580
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