Tag | Content |
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EnhancerAtlas ID | HS089-07610 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr2:113756270-113757020 |
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) |
HES2 | MA0616.2 | chr2:113756570-113756580 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr2:113756570-113756580 | GGCACGTGCC | - | 6.02 | ZNF263 | MA0528.1 | chr2:113756745-113756766 | GAAGGAGGAGTGGGTAGGAAG | + | 6.44 |
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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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Enhancer Sequence | TCATGTCAGT TTGGGTGCTT TGATGAGAAG ATGTTAAGAG ATTTAATGGG AGACATGCCT 60 GAAGGCCAAA AAAGAGGGAT CAGGAGTAGG TAGGGAGAGC ATTCAGACTG TGAGGCAGGA 120 CTGACACCAA TGATAGAAAA GAGAGAAGGA AAGGCCAGGT GCGGTGGCTC ACACCTATAA 180 TCTCAGCACT TTGGGAGGCC AAGGCAGGCA GATCACTTGA GGTCAGGAGT TCGAGACCAG 240 CCTGGCCAAC ACAGTGAAAC CCCACCTCTA CTAAAAATAC AAAAATTAGC CAGCCATGGT 300 GGCACGTGCC TATAGTCCCA GCTACTTGGG AGTCTGAGGA AGGAGAATCA CTGGAACCCA 360 GGTGGAAGAG GCTGCAGTGA GCCGAGATCA TGCTACTGCA CTCCAGCCTG GGCAACAGAG 420 CATCTTGAGA CTCTGTCAAA AAAAAAAAAA AAAAAGAGAG AGAGAGAGAG AGAAGGAAGG 480 AGGAGTGGGT AGGAAGAGCG TCAGACTGCA GTGCACCTGT GAAGCTCTGA GAAAGTCTCA 540 ACCTGGCACA TTGGGGAGCC CTAGAGCAAA ACTTGGCTGC AGAGGCATTC CACATCAGTA 600 GGAAAGACTG CCATCACTGG CTGGGAGCAG CCCAAGAAAA GAGTGTTCTT GGCAGGAGCA 660 CTGCCATGAA TCCAAAATTG CAGCAGCTGA GGTTGTCTTC CAACTGTTCT CCTTGTAACA 720 GGTTCTTTTA AAGGGAAGTC TGAGAGTCAC 750
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