Tag | Content |
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EnhancerAtlas ID | HS098-02291 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:67805140-67806480 |
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) |
MEF2A | MA0052.3 | chr1:67805873-67805885 | ACTATAAATAGC | + | 6.11 | MEF2B | MA0660.1 | chr1:67805873-67805885 | ACTATAAATAGC | + | 6.74 | ZNF263 | MA0528.1 | chr1:67805806-67805827 | ATTTCTTCTTCTTTCTCCTCC | - | 6.25 |
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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 |
GH01I067339 | chr1 | 67805134 | 67806903 |
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Enhancer Sequence | GCTTGGGTGA CAGAGTGAGA CTACGTTTCA AAAAAAAAAA AAAAAGAAAA TCATACAAAC 60 AGGAATAGAA AGCAGCCCTT CCTCAGGAAT GGTAATAAAA CAGTAGTAAA TTAGACAACT 120 TTCCAGAAAA CAGTGAAGCC TGACATTATC ATAGAATGCG AAAGTTTCAC AAAGCACTGA 180 AAGCTGGCAT TACCATTTTA TTTAATCCTC ACAAAAATCC CCTGAGGTAA GTACTGGTAC 240 GCCCACTTAC CAGTGAATGA GAAAACGAAT GAATGAGTGA ATGAAAAAAC GAGTATCAGA 300 GAGAGGAAAG AGAGGAAGTT CTTGCCCAAA GTCACCCAGC TACTGAGCAC AGACCTGAGA 360 CTGAAACCTT ATCCAGAACT GCTGCATCGT GACTCATCTT TGTTGAAGGA AAATGCTGTG 420 CGATTCGAAT TGAGCTACTG ATTGGCATGC TCATAAGAGG TTTCCTGGTG AACTGCACTC 480 TTTATTTCTC AGGACTCACA TCCTCTTCAC TACACCTCTT CCAGTTGAGG ATAGAAAGTT 540 TTGGAATTAT GAATCTGAAT GAGCACAAAA CCAGAAGAGT AAGAATAACA ATTATAAAGT 600 CCTCTGATGG GGTTCACATG ATGGGTTTTG ATCATTGCAC ACTTCTTCAG TTTTAAGAAA 660 TGAGTGATTT CTTCTTCTTT CTCCTCCCTG TCTCTCTCAC ACACACATAA AACGTCTGGT 720 ATAAGAAGAG ACTACTATAA ATAGCCTGGT GAATCATGAT CAGGCTCTTC ACTTTGAAAC 780 TAACACTGCA GCTCAAAATT TATTTTAAAA TGAATCTACT TTCAATAGCA AGACAATTCT 840 CAAAGCAGGA CATTTAGAAC AGCCATAATT TGTGAATATT ATAGAAGAAC CCAGCCTAAT 900 TATTTCCTTT TCACGAGCAA GTGACTGGTT AAAACCAAAA TTCCTCCTCT CATGTAAAGG 960 TTTCTCCTCC AAAAATGTCC TCAACAGTGA TCTGGAAAGA TATGCTACGT GTTAATCTAT 1020 TCCACGCCTC TCAACTCAAG GGTTTCTCTC AGTAGAATGA GGGTAATGAT ACAGGTATCT 1080 GCAAAGCTGA CAAGACCATT GTGGGGATCA GCAAATGAGA GGACACAAAT GTAAAAATCA 1140 CAAGGGCCAC CAGTGTAAAA TTCAGCAGTG CTGCATGATG CGTGTTTATC CTGACAGTGA 1200 AAGCTCCATG CCTGCGTGCT TTTCACTGTA ACAAACAGAG TTTATAGTGG ACATCATCTT 1260 GGTTCTCTGA AACCAGCACC AGAGTGAAGT CAAAATAAGT ATGTGTTGGC CATGAGTGAT 1320 GCTTGGTAAA TGTGAGTATG 1340
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