Tag | Content |
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EnhancerAtlas ID | HS091-36539 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr4:38450250-38451560 |
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) |
Myod1 | MA0499.1 | chr4:38450509-38450522 | TGCAGCTGTTCCT | + | 7.34 | Myog | MA0500.1 | chr4:38450508-38450519 | CTGCAGCTGTT | - | 6.02 | Tcf12 | MA0521.1 | chr4:38450508-38450519 | CTGCAGCTGTT | - | 6.62 | ZBTB18 | MA0698.1 | chr4:38451082-38451095 | CATCCAGATGTTA | + | 6.42 |
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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 |
GH04I038449 | chr4 | 38450932 | 38452655 |
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Enhancer Sequence | GACCATTGGA AAAGTGCAGT ATTAGGGTGG GAGTGACCCG ATTTTCCAGG TGCCGTCTGT 60 CACCCCTTTC TTTGACTAAG AAAGGGAATT CCCTGACCCC TTGCACTTCC TGAATGAGGC 120 AATGCCTCGC CCTGCTTCAG CTCATGCTCG GTGCACTGCA CCCACTGTCT GACACTCCCC 180 AGTGAGATGA ACCTGGTACC TCAGTTGGAA ATGCAGAAAT CACCCATCTT CTGCATCACT 240 CACGCTGGGA GCTGTAGACT GCAGCTGTTC CTATTTGACC ATCTTGACTC CACCCCCCTT 300 AAATTTTTAT TCTAATGCAC ATTAACGTAA ATATCACACT ATTTTTTATG TCTATTTATA 360 TTCACCTGTT TTGGCGTGAA AGGTAATATT ACGTTGAAAA ACATCTTTTT TTTTCTCTTT 420 TAGTATTAAA CTTTTATTTT AAGCTCAGGG GTAGATGTGC AGGTTTGTTT AGATAAACTT 480 TTGTCATGAG GGTTTGTTGT ACAGATTTTT TTTTTTTTTT TTCTTTTGGA GATGGAGTCT 540 CACTCTGTCA CCCAGGCTGG AGTGCAGTGG TGTGATCTCG GCTCACTGCA ACCTCCACCT 600 CCCAGGTTCA TGCAATTCTC TCCTGCCTCA GCCTCCTGAG TAGCTGGGAT TACAGGCACA 660 TGCCACCACG CCTGGCTAAT TTTTGTATTT TTACTAGAGA CGGGGTTTTG CCATGTTGGC 720 CAGGCTGGTC TCGAACTCCT GACTTCACGT GATCTGCCTG CCTCAGTCTC CCAAAGTGCT 780 GGGATTCCAG GCATGAGCCA CCATGCCTGG CCTGTTGTAC AGATTATTTT GTCATCCAGA 840 TGTTAAGCCT AGTGTACATT AATTACGTTT CCCAATCCTC TCCCTCCTCG ACCCTCCACC 900 CTCTGCTGGG CCCCAGTGTC TGTTGTTCCC CTCTCTGTTT CCATGTGTCA ACATCACACT 960 ATTAACATTT GTAAATGTAT ATCTGTGTAT CACCCCCAAA TTATCATGCT TACCCTATGA 1020 GTACCCGTAC CACAGATTGA GCAAAACCAG CTTTAAGTAC TCAGCTCGGC TGCCCTGCGT 1080 TAGTCACCTC CCTCCACCAG TGCATACCAT GAGCATAAAA TAGTTTCTGG GAGGTCAGTG 1140 ATTCACTTGG TATTTACTTG TTTTCTAGAC TTTAGGAAAA AGGAAATCTT TCTATATGAA 1200 AATCATGTAC ACATCTACAG AAAACCTCAT CTTTGTTGTG TTCCAGAGCT TTAAAAGCAA 1260 GCAGCACATC TGCTGCAACA TCCTCTCATG CCTGCATCAG AGCCTGGAGC 1310
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