Tag | Content |
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EnhancerAtlas ID | HS193-03946 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr10:26695960-26697420 |
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) |
HNF1A | MA0046.2 | chr10:26696203-26696218 | AATAAATTATTAACT | + | 6.8 | HNF1B | MA0153.2 | chr10:26696204-26696217 | ATAAATTATTAAC | - | 6.11 | JUN | MA0488.1 | chr10:26696983-26696996 | ATGACATCATCTA | - | 7.12 | JUND(var.2) | MA0492.1 | chr10:26696982-26696997 | TATGACATCATCTAA | - | 7.21 |
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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 |
GH10I026407 | chr10 | 26696441 | 26696722 |
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Enhancer Sequence | ATATTATTCT CTTTTGTCTC TTTTTTTCCT TAATCAGGAT TGTCAAGGTT TTATTTTTAT 60 TTGTTTGAGG GTTTTGGTTG CTTTTTAAAA AAGTAAAAGC CTGTTGTCCC AGCTACTTGG 120 GAGTCTGAGG CAGGAGGATC ACTTGAGCCC GGGAGTTAGA GCCTGTAGTG TGTTATAATC 180 ACATCTGTGA GTAGCCACTC CATTCCAGCC TATGCAACAT AGCAAGACTC TGTCTCTAAA 240 AAGAATAAAT TATTAACTGA AAGTAAATTA AGAAACAAGT ATTTGTTGTA ATTTACATTT 300 TCTGAAAAAT ATTTATTTTT ATTAATTTCA ACTATCCCTT TCCATCATCC TACTTTCTTT 360 TCATTCATTT TCCTGATGTT TTAAAATTTC TTAATGTTGG GCTATTGCGC CAGCTGAATA 420 TGTGGAAGGC AGGAGCCTGG AGGCCAAGCT TAGCTGCCTT CCATGCTCCC TTTACATCTT 480 CCCTCTGTGT GCCTGTCCAC AGTGAGTCAC GCATGAGAAG ACAGACTGAA GAGAGCAGAG 540 GGCCCAGGCC TGGAGGAATA GAGTCTAAAG GGATCCCATG ATCAGTTAGT CATCATCAAA 600 GGTCCTTGCA AGTCAAACAT TCTAATTGAT GTTTTTAGTA ATGGCTCACT AGCAACCCTT 660 CCCTTGACAA CTAGTAGAAA GCAAACAAAA TATTTTTGAA ACCTCTTACA GACATAGAAG 720 GCACAGAGAA GGTACAAAAG TAACAAGCAC TTGAGAATGC AAGATTGCAG AAAGAAGGGA 780 TGTATAGAAT TCCATATTCA AGCAATTATT CCTCTTGAGG GATTTGCTGA TTAACAAACT 840 GCAATTAGGT CAGAAACTGA GGAACTGACA CTCTTACTGA GATGGGAGAC CAAATTAAAG 900 TGAGAACCCA GCAAACAAGA GAGATTTAAA GGGATATTTC AGCTTTTTCA GTGGGACCCC 960 CCCAAGATTC CTAAAGGACT GCATCCGGGA GTGGGTTAGA AATAAATCAG AACTCAAAGG 1020 ACTATGACAT CATCTAAAGG CTCTAATGAT ATCTACAGCT GTTTTTTTTT TTTTTTTGCA 1080 ATGCCCACCA TTCAATCAAT TACCTCTCAT ACCATAAATA AGACCACATG CCCCCCAAAA 1140 TTATGAGCAT TAAACAGACC CACAGGAAAT TACAGATATC GGGGGCATCA GACACAGGTT 1200 TTAAAATAAT TATGATTAAT ATGTTCAAGA AATGAGATGG CATGATGAAG AAACTCAGTA 1260 GAGAACTGGA AACTGATCTT TAAAAAAGAC AAGAGAAAGG AGGGGAAAAT ATAAAAGTCA 1320 ATCTTAACAG TTTGTGCAGT ATCTCTTATC TGCAGACCAC GGGATTTATA TTATTGCACT 1380 CTTGGTGCAA CTTATAGTAT GTATGTAATA GCTTTTATGA ATTGTTTGAG TTATGAATTT 1440 CTATACCCTC TATTAAAATG 1460
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