Tag | Content |
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EnhancerAtlas ID | HS043-42027 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr8:102702070-102703680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2F1 | MA0017.2 | chr8:102702742-102702755 | CTTTTGACCTCTG | - | 6.59 | ZNF263 | MA0528.1 | chr8:102702420-102702441 | AGAGGAGGGGAGGGGGTGGGG | + | 6.55 |
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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 |
GH08I101689 | chr8 | 102701553 | 102704615 |
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Enhancer Sequence | CTGGAGCCTT CTGAGCCACT TCGTGTTCTT CAGGCCACTC TGTGTTCTTA GGTTTGCTGC 60 AAGAGCCCAT CCTATCTTGG GGAAGAAGCC GTGGACGTAA GTGTTTGTTC ATACACCACG 120 GGAAGACAGC TGTGCCTCCA TCTGAGGTCA GGGAAGAGCA GGGTATGTTC AAGGCAGAGG 180 GTAACCCATG GGTTTCTGCC TCTCAGTTAG GGTGCTCTCC TGCTACCCTG ATGTGCTGGA 240 GGAGGGAGGC TCAGCAGCCT GGGCTCCCAC TCCGACCCCG GTGACCTTTC CTTTCTGCTT 300 ACTCTGGAGC ACGTACAGAA TTCTCTTCCA GGAAGGCCTG TCACTTGTGG AGAGGAGGGG 360 AGGGGGTGGG GTAGGAGTTG GGGGACTGCA AGGCTTTTCC CATTCCTGGT GCTTCCAGAA 420 GGACCCTTCC TCTTTGTCTA CCCCGCCCCT GGGAGTGAAG TGACATGCTC GATTGGTAAA 480 TTTGGGAGGA ATTGCTGGGC ATCTCCGCCC AGCTTTGCCC TCCCTTTTTC TCTTGAAAGG 540 AGCTGCCCCA GAGAGGATTT ATTTCCATCT GCTCCTCCAA GGGCAGCACC CGGCCTGCCT 600 GGCTCTGCAC GCCTGTGGGT TTTTCAGCAC GTCCTTGGAC TCTCACGCTA AGCCATAGCC 660 TCCAGTATCT ATCTTTTGAC CTCTGTCCTC TTTTATTTCT CAACTTACTC CAAACCTGAC 720 AGGAGGGGGC CTCCCCCAAC AGAAACACCA ACAAACATAT CTTCTCCTCA GCCACAACTC 780 CCTCCCCGCC AGAACCTAGT TCTTGTTTAA TGAAACCCAC TTTATCTCCA TGAAGGAAAA 840 AGATAGGGAT GCATTTATTA ATTTATTTTT AATTTGTAGA GCTGATCCCC TCCAAGCTCT 900 GTGTGCTGGC CATTTTTTAT GAGCCCAGCC CTGCCCACAT AGTAGTTACA ATGGTAATGA 960 CTTCCTCCAG CTTGGCAAGG CATGAGGGAA GGGAGACAGG CGTGATCTCT GAACACTTTG 1020 CAGTCTCTCA GGGGTCGGCT CTGGGAGGCA CCAGCTGGAG GTAGCAGGGG CAGACCTGGA 1080 GCTCGGCATG ACGTCTGGCT TTCTTCACTT AACTGTCTGC ATGATTCAGA GTTGGCTCCT 1140 AGGAGAACTT GCCTGAGGGC CCAGATTTTT CTTTTCAAAT CGGAGGCCAG AAGTTAGATT 1200 CCAAGAGCAA CAGGCAAGCT AAATCTAAGG GTAGGAGACT CTAGGTGAGG ACTGCTCTGC 1260 TCTCGGCAGG GAGGGGTGCA GGTGTCCTCA ATCCTGGGGT CCAGCAGCCA AGCACTGAGC 1320 TGAAGCACCC AGTCTCCTGG TTGAGCTAAG ATTCCTCTGA CAGCTGTGAA CTTACAGCCC 1380 CTCTTCCTCC TTCCTTCTAC AGCTCCCACC CCCCTCTCCC AACCCTAACC TTTGAAAATT 1440 TAATTTAATT TTAAACATGA GGTTTTCCTT TGGAAAGGCA CAGGTCTTTA GCAGTAAGTT 1500 GTGCTCTGAG AATGCTAACT CAGTCAGGGC TCTGCAATCC CATAGCAGCA GAGTCCCAGT 1560 GGAAAGACCC TAATTCATTG CCTGTGATCA ACACACAGTT AGGGCTTTAG 1610
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