Tag | Content |
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EnhancerAtlas ID | HS052-36251 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr8:8502520-8503610 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr8:8503411-8503425 | AGTCCCCAGGGAAC | + | 6.41 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 8502577 | 8503352 | chr8 | 8503496 | 8503599 |
| | Number: 1 | ID | Chromosome | Start | End |
GH08I008645 | chr8 | 8502691 | 8503431 |
| Enhancer Sequence | CTAAATGCAT GTCATTTTCA CACCATTGTA AATCAAAAAA TTTTAAGTCA AAAGTATTGT 60 AAGTCAGGAA CTGTTTGCAC CCATCTGAGG ACAGAAGCAA CACTACAGCT GTCAGTAATT 120 CAGGTTCCAT AGCAGAAGGA ATAATGACAG CTTTCATGTG CATATAGATG ATGCGTATAT 180 GTGGACCAGC CAGTGTTAGA GCTGGAGTCA GAGGACTGTG ATGTCAGTTC CAAATCACCA 240 AAAAGAGGCG AGCCAATGCC TGTGTGGCCT GGAAAACACA TCTCTGTGGG CTGGCAGCCA 300 GCATGAGAGA AGCACAAGCT GTAACACCAA GAGGTTTACA GAGTCCCCAT GAGAGGGTGG 360 CAGAAGCACC TCCAGGCTCC CACAGGGGCC CCAGTGCCTC TACCACAATC AAAGCTGCCC 420 CTAGCCCTGC AGTGCCCTCG GTGGACACAG ACGCAGGGAG GCTGACTCAC TCACGCTCCA 480 GTATGGAAAG CCAAGTGTCA ATGTATTCAT TTCTACCAAG GGATGTTTCT TTCCAGCAAC 540 AAAAATACCC CATTGCCTAC CAAGGGCCCA GAGCCACTGC CTCCTGACAT TAATCAGAAG 600 GATGCGTCAT GAGCATGGAG TGAAGCCAGA TGCAGCACGA CACAGTGGCC TCACTTACCC 660 CACTGTGGTC AAGCCTTCTC ACTGGGTGGT CCACATGAGG GTGTTGCTCT CCTCTGGACA 720 TTGGTGGGGC ACTGCCACCC TCTGCCTCTG CCTTCCCTCA CCTGGCCCCC AGGCTGGACA 780 CCCATTTATG TTCATACAGC CTTTCCCACA AAGGCCATAG TGAGATCTCA AAGGTCTGAT 840 TCAAATGTGC CAAGGGAGCC AGGGAAGAAT GGGGGAATGG TGGTCTCTGA TAGTCCCCAG 900 GGAACTGAGA AGATGCTTCC CATCTACCTG AGAAAATTAA GAAACCCTGA ACCTTCCCCT 960 CTTCCATATC GCCCAGCAAT CCCAGGCCAT ACCCCAAATC CACCCCTTGG GTCACACCTC 1020 AGGGGTTCAC ACCACAGGGG TTCACACCTC AGGAGATCAC ACTGCAGGGG TTCAAACCCC 1080 AGGGGAATCA 1090
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