Tag | Content |
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EnhancerAtlas ID | HS091-01587 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:45825460-45827030 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:45826961-45826982 | CTTTGCTTTCATTTTCAGCTA | + | 6.79 | IRF2 | MA0051.1 | chr1:45826960-45826978 | GCTTTGCTTTCATTTTCA | - | 6.31 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 45825721 | 45827000 | chr1 | 45826121 | 45826507 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I045359 | chr1 | 45825474 | 45827561 |
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Enhancer Sequence | TGGAGGCAGA GGTTGCGGTG GGCAGAGATC ATATCACTGC ACTCCAGCCT GGGCAACAGG 60 GTGAGACTCT GTCTCAAAAA AATAATAATA AAATAAAATA TGTGAAAGCG CTTCGAAAAA 120 AATTTAAATG TCATATATTT TCTGATGTGG TAATAATATA AGCACCAAAA AGAACCAGTT 180 GGGGGCAGCA CCATGCAGCA CTTCAGATCC TTGGAAGCGT CGGACCAGTT TTGGCAAGAC 240 AGAAAGAATG ACTAAAAATA AATCTTCCAA CTTCTCAAAA GGGAAACTTG TTGATCTGCT 300 TCATCCTGCT TGATAATCCA TCTTTGAAAA TCTTAAAATA AGGCATAATG ACGGCATAAG 360 CACAGCGCCT TGCTCTCTTC ATTCTAGTTG AATCTGCCCA AGATTCACAT TTGAGGTGCC 420 CATTTGCTGA AAAGAAACTG AGCTTGTGAA CTTCAGGGTT ATAAGTGGGC AGTGAAGCTG 480 ACATCTAATC ATGCAGGCAG ATTTCTTTAG CTCTGAAAGT CAAAAGGTAG GCAGTGGTTC 540 ACTTCTTTAG CATGATGACA GTGTGATATG TCGGGCCTGT CTTCAGGAGC CACTCAGGTT 600 TCCCAACTGA GTGCCAGGCA GAAGACACTA TAATGAAAAG ACTGTATGTG CACTCTCTAT 660 AGGCCAGGTG ACACCAGGAC TCTTGGTTCT GGGAAACACT TGTTTACTCT GTTCAGCAGT 720 GTCTCTGAAG GCCCTGGAAA TCCATATGCA AAGCCAGAGG GTGGAGAGCA CAGGAAAAGG 780 TGACAAAAGA TGAGGAATCA CACTTGGCTA ATAGATTCTG GCTTCTCCAG GCAAACTGGA 840 AAAAGCGCAA ACCAAGGACC AGAGAGGGAA AACAAATGGA ATTTGCTTTT ACAACCCATT 900 TCTCTTGCCT GCCTTTGGTG AATACATTAG TTGGGCTGAT AAGCCTGTAG GCCCTCAGAA 960 ACCGCTTCTC AATGTTTCAA GACCTCTGCA TGCATAAGAA AAGGAAATTT GAGATTTGTC 1020 AACAAGGAAG ATTTCTTTCT TTTTTTTGAG ACGGAGTCTC ACTCTGTCCC TCAGGCTGGA 1080 GTGCAGTGGC GCCATCTCGG CTCACTGCAA CCTCCACCTC CCAGGTTCAA GTGATTCTCC 1140 AGCCTCAGCT TCCCGTGTAG CTGGGATTAC AGGCTGTGTC ACCACACCCA GCTAATTTTT 1200 GTATTTTTTA GTAGAGACAG GGTTTTCCCA TGTTGGCCAG GCTTGTCTCG AACTCCTGAC 1260 CTCAGGTGAT CCACCCGCCT CAGCCTCCCA AAGTGCTAGG ATTACAGGCG TGAGCTACCG 1320 CACCCAGCCA GAAGATTGCT ACACGGTCTC TGTGCCCATT AGCTGGAATG TTCACTTCTC 1380 CATAAGCAAC TCCCAGTGCA GACTCAGCTG GTGTGGCCTC TAAACAAATC CCTCTGCAGG 1440 AAGCAGAGAC AAGAGCAACT GCATTAGCAT GTTCAGCTTT CCCGGATGGG GATAACAGCT 1500 GCTTTGCTTT CATTTTCAGC TAGACTACTC CCTCGGTCAG CCCTATAAAA TGACCCAAGG 1560 CATTGGTAAT 1570
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