Tag | Content |
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EnhancerAtlas ID | HS012-00775 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr1:175953620-175954860 |
Target genes | |
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) |
HNF4G | MA0484.1 | chr1:175954136-175954151 | TGGACTTTGGACTTC | - | 7.07 | MEF2A | MA0052.3 | chr1:175954266-175954278 | TCTAAAAATAGT | + | 6.02 | MEF2C | MA0497.1 | chr1:175954264-175954279 | ATTCTAAAAATAGTT | + | 6.25 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I175984 | chr1 | 175954061 | 175954210 |
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Enhancer Sequence | CTCATGGAGA ACCTCTGCCA CGGCAGTACA GAAGGGAAAT GTGGGGTGGG AGCCCTCACA 60 CAGAGTCCCT ACTGGGGCAC CACCTATGGG GCTGTGAGAA GAGGGCCACC ATCCGCCAGA 120 CCCCAAAATG GTAGATCCAC TGACAGCTTG CACCGTTCAC CTGGAAAAGC CACAGACAAT 180 GCCAGCTCGT TAAAGCAGCC AGGAGGGAAG CTGTACCCTG CAACGCCACA GTGGTGGAGG 240 TCTCCAAGAC TACGGGAACC CACCTCTTGC ATCAGTGTGA CCTGGGTGTG AGACATGGAG 300 TCAAAGGAGA TCATTTTGGA ACTTTAAGAT TTGACTGCCC TGTTGGATTT TGGACTTACA 360 TGGGGCCTGT AGTTTTGTTT TGGCCAATTT CTCCCATTTT GAATAGCTCT ATTTACCCAA 420 TGCCTATATT CTCTTCATAT CTAGGAATTA ACTGATTTGC TGATGATTTT ACAGACTCAT 480 AGGCAGAAGG GACTTGGCTT ATCTCAGATG AAACGTTGGA CTTTGGACTT CTGAGTTAAT 540 GCTTAAATGA GTTAAGACTT TGGGAGACTG CTGGGAAGGC ATGATCAGTT TTGAAATGTG 600 AGGACATGAA ATTTGGGAGG GGCCAGAAGC AGAATGATAT TTTCATTCTA AAAATAGTTT 660 CCAGTTCTCA GTTAAAATTT TCAATCTTGT CTTTCATCTT GTAAGCATAG CTACTTTCAA 720 GCTGTCTGAT AATTTCAATA TTTAGAGCTG CTGTGACTGT TTCTACAGTC TGTTGCTTAG 780 GCTGGTTTAA TTCATGCTGT CTTCTCTTTT ACTATGTCTG TTTATTTTTT ATTGTGCCCT 840 AGTTATTGTA GTTACAAAAC TAAAAAAAAT AAAGCACTTA GATGATCTTA TCTTTTTTCA 900 GAGGATTTAA GTTTGCATCC TGTGGATATT AGCAATCAAG GGTCACCTCA ATTCAATTTC 960 AGAGATTGAT ATGAAGTTCA GATGCAATCG CTATGAAGAC TTATCTTCTG GTTTCCCCTA 1020 TAATATACCC CTGTGGGGAC TTAAAACAAA GTAATCACCC ATACAACGTC AGGCACTGAG 1080 CTCCAATCCC TGCAACCCTG TGAAGCTAGT ATAAGCACTT TCACCCACCC CACCAGAACT 1140 GACAAATGCT CACAGGGGAA AAGTAGATTC AAAAGCCAGG GTCACAATCC AAATCTGGTA 1200 ATTCTTTCCT GTCTTGTTTG CTTTCCAATG CTTTCAAATA 1240
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