Tag | Content |
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EnhancerAtlas ID | HS118-01028 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:119456800-119457990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:119457809-119457827 | CTCAGGAAGGAAGGAAGG | + | 6.47 | EWSR1-FLI1 | MA0149.1 | chr1:119457813-119457831 | GGAAGGAAGGAAGGCACT | + | 7.27 | HNF1A | MA0046.2 | chr1:119457205-119457220 | AGTTAATAATTAATA | + | 6.19 | HNF1A | MA0046.2 | chr1:119457205-119457220 | AGTTAATAATTAATA | - | 7.09 | HNF1B | MA0153.2 | chr1:119457206-119457219 | GTTAATAATTAAT | + | 6.98 | NEUROG2 | MA0669.1 | chr1:119457693-119457703 | AACATATGTC | + | 6.02 | NFAT5 | MA0606.1 | chr1:119457104-119457114 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr1:119457104-119457114 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr1:119457104-119457114 | AATGGAAAAT | - | 6.02 |
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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 |
GH01I118914 | chr1 | 119457421 | 119457570 |
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Enhancer Sequence | ATCTGGAAAC AAACAAATAA GTATGAATTG CTTTTATATT AACTGATTTC TTTCTTAGTA 60 CTCCTAGAAA ATTACAAAAA TCACTTTTTT AATAACAGTT GTTGCTTTTA TTTAATTTCC 120 TTTCAGCTCA AGATTTAATT TGAAGCTGGA TATAGAACTT GGCCTGGCAC ACAGATGTCT 180 GACCCACCCG ACTCACTTCT CTATAAAAAC TAAAATTTGC CCAGTATGTG ACTCTAAAAA 240 CTCTCTCCTA CTCACCTTCC TTGCCCCAGA GTGGTGGTAA ATCACTTGCC TAGACAGATA 300 TTGAAATGGA AAATTGGTCA ATGGTCACGT CCATGGTACA TGACACACGG GAGGCACTTA 360 AAAAATGCTT GTTGAATGAG TGAGTAAACA AATGATGTGT AAGTGAGTTA ATAATTAATA 420 ATGGACTCAG TCAATTCAGT TAGGTGGAAT CAGACCACAA GACAATCTGC CTTAGCCTGA 480 AAGACCCAAA AAATTGACTG CATTTGCCAT TTCACTGAAG GCATGCCTTT CCTACCACTA 540 GAAATTATTC ATTTAATGAC TTGAAATGTT CATGTAGAAG ACAGAAAAAG CAGACTTTTG 600 CCAGGGTCTT ACCCAAAGGA AAATCTACAA TGTGAGACTG AATGGGGCAG GATGCAGTAC 660 ATGTTATCCA GTCTCCAAGA CTCACAAGCA AATCAGAAAC AAAGAGCCAG TTTCATAAGG 720 CTGACCAAGC TAGCACATCC AATTGTGTCA CCAGCTTGGT CCTCAGGGGC CATGTGGTTC 780 AACCCCCACT CAATGCATAA GTCCCCATCC ATTGCATCCT ATCTTAGTTC TGGCAAACCC 840 TGCCATGGTT GTATATATTG CCCTCATGCC TGTAGACTAG AACAAGCCTG AACAACATAT 900 GTCACATGCA CTCTAGTGTT TCCACTTTCA GCCTTGGTAC CTTTGTGTCT GAATTGTTAA 960 TGACTCACTA CATGCAAGCA ATGGAGACTT AGGCATAGGT GCTAGGGAGC TCAGGAAGGA 1020 AGGAAGGCAC TCCCAATGCA AGGTGATTCT AGAAATAAGG GAATCTCATT ATTTAAGACC 1080 ATCTTCATAT TTTTGATAAT TGTAGAACGT ATCACTAGGA CAGCTAAAGT TGTTTCCTAC 1140 ATTGCAAATC TTTCCTAGTT CTCTTTCACC TCATTTTATC AGAGTGGAAT 1190
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