Tag | Content |
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EnhancerAtlas ID | HS139-52472 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr8:8502370-8503970 |
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) |
EBF1 | MA0154.3 | chr8:8503411-8503425 | AGTCCCCAGGGAAC | + | 6.41 |
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| 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I008645 | chr8 | 8502691 | 8503431 |
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Enhancer Sequence | GAGCTATCAT TGTGCCACTG CACTCCAGCC TGGGCAACAG AAAAAAAAAA GAAAGAAAGA 60 AAGAAACAGA AAATGTGTGT TTGACTCACA GTATTTTCAA CTTTTGATAG GTTTATCCAG 120 ATACAACCCA ATCATAAGTT GGGGGGTGAA CTAAATGCAT GTCATTTTCA CACCATTGTA 180 AATCAAAAAA TTTTAAGTCA AAAGTATTGT AAGTCAGGAA CTGTTTGCAC CCATCTGAGG 240 ACAGAAGCAA CACTACAGCT GTCAGTAATT CAGGTTCCAT AGCAGAAGGA ATAATGACAG 300 CTTTCATGTG CATATAGATG ATGCGTATAT GTGGACCAGC CAGTGTTAGA GCTGGAGTCA 360 GAGGACTGTG ATGTCAGTTC CAAATCACCA AAAAGAGGCG AGCCAATGCC TGTGTGGCCT 420 GGAAAACACA TCTCTGTGGG CTGGCAGCCA GCATGAGAGA AGCACAAGCT GTAACACCAA 480 GAGGTTTACA GAGTCCCCAT GAGAGGGTGG CAGAAGCACC TCCAGGCTCC CACAGGGGCC 540 CCAGTGCCTC TACCACAATC AAAGCTGCCC CTAGCCCTGC AGTGCCCTCG GTGGACACAG 600 ACGCAGGGAG GCTGACTCAC TCACGCTCCA GTATGGAAAG CCAAGTGTCA ATGTATTCAT 660 TTCTACCAAG GGATGTTTCT TTCCAGCAAC AAAAATACCC CATTGCCTAC CAAGGGCCCA 720 GAGCCACTGC CTCCTGACAT TAATCAGAAG GATGCGTCAT GAGCATGGAG TGAAGCCAGA 780 TGCAGCACGA CACAGTGGCC TCACTTACCC CACTGTGGTC AAGCCTTCTC ACTGGGTGGT 840 CCACATGAGG GTGTTGCTCT CCTCTGGACA TTGGTGGGGC ACTGCCACCC TCTGCCTCTG 900 CCTTCCCTCA CCTGGCCCCC AGGCTGGACA CCCATTTATG TTCATACAGC CTTTCCCACA 960 AAGGCCATAG TGAGATCTCA AAGGTCTGAT TCAAATGTGC CAAGGGAGCC AGGGAAGAAT 1020 GGGGGAATGG TGGTCTCTGA TAGTCCCCAG GGAACTGAGA AGATGCTTCC CATCTACCTG 1080 AGAAAATTAA GAAACCCTGA ACCTTCCCCT CTTCCATATC GCCCAGCAAT CCCAGGCCAT 1140 ACCCCAAATC CACCCCTTGG GTCACACCTC AGGGGTTCAC ACCACAGGGG TTCACACCTC 1200 AGGAGATCAC ACTGCAGGGG TTCAAACCCC AGGGGAATCA CAGCACAGGG TTTAACACCC 1260 CAGGAGATCA CACTTCAGGG TTCATACCTC AGGTGATAAC ACCGCAAGGA TTCACAACTC 1320 AGGAATTCAT ACCTCAGGGG AATCACACCA CAGTGGTTCA CACCTCAGGG GATCATACCT 1380 CAGGGGATCA CACCGCAGGG GTTAACACCT CAGGGAATCA CACCACAGGG GTTCATAACT 1440 CAGGGGATCA CACCTCAGGG GTTCACACCC CAAGGGAATC ACACCACAGG GGTTAGCACC 1500 CCAGGAGATC ACACTTCAGG GTTCATACCT CAGGTGATAA CACCGCAAGG ATTCACAACT 1560 CAGGGATTCA CACCTCAGGG GAATCACACC ACAGAGGTTC 1600
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