Tag | Content |
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EnhancerAtlas ID | HS053-26954 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr3:48068200-48069560 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
mix-a | MA0621.1 | chr3:48068284-48068295 | AATTAATTAGT | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATTAAGTTAT GCCATTATCT TATGCAGTTG ATTTTAAGTG ATGAACACCC ACCTACATCA 60 TTATTTCCAT ATAGAACCAC CAACAATTAA TTAGTTCAAA CTAAAAATAA TGAAATAAAG 120 TATTAAAATG TTCTCCATAA CTAAGAAAAT ACTGTCACTG TCAGCTTTAC TATTTCTACC 180 CATCACCACG ACTACCCCCC AAAAACCCTA CATATCAATA CAGCTTTCAT CAAATTAGAA 240 TCAATTTGCT TGAAAAAACA GAAACATATG CATCACCCAT TACTATGTAC ACATCTGCCA 300 GATAATGATT AGAGGCGGCA AGTATGCCAA GAGTCCAAAA AGCAGGTGAG AATCTTCTGT 360 AGCCTAGAAA AAAGTGTATC TAGAGAAAAC ATAATAGTCT CCTCTATTCC CAAAGCACTT 420 AAGACTAGTA AGACTTCCTG AAGTCTCCAA CTCATAAATG GTCATTGTTT CACAGCTCAA 480 GTAAATACAT GTATGAACAT GTAAAATAAA AAAGAGTAAG GGAGAACCTT AAATTCTCCA 540 GTTTACTCTC AAATTTTAAA ACTCAGAAAA GAGAGATCCA AAGTGGTTTC CCTTTGCCAA 600 AAGCCATCTA GAAAACTAGA GACAAAGCTA CAATTAGGAC AAACATCTCC CAACTCCCAC 660 CAAGCCCAGA GTTCCCTCCC CAAAATGAAT ACTCACTGAA CCCACAAGAG AAGCACCAGT 720 TCAGAGTGCA AACCTAGGTC AAACAGGCCC CTTGGTGCAG TGGCCCATAT AGTGTTTTGA 780 AAAATGGCCA ATATCTCCAA AATCAGTAAT CTTTGAATGA AAATACAGTT TTACAGCTTT 840 TTTAAAAAAC AGGGCCAGGC GCGTTGGCTC AGTCCTGTAA TCCCAGAACT TTAGGAGGCT 900 GAAATGGGAG GATCCCTTAA GCCCAGGGGC TCGAGACCAG CCTGGGCAGC ACAGTGAAAC 960 TCCGTGTCTA CAAAAAATAA AAAAAATTAG CCGAGCATGC ACCTGTGGTT CCAGCTACTC 1020 AGGAGACTAA AATGGGAGGA TCGTTTGAGC CCGGGAGGTC AAGGCTGCAG TGAGCCATGA 1080 TTGCGGAACT GCACCTCAGC CTTGGGTGAT AGTGTAAGAC CCTGTCTCAA AAAAATAAAA 1140 AATCCGAAGA TCAGGCCATG ACTATGTATT TCCACTTAGC AACAATATAC TGGAGCTGAG 1200 AAATAACTGC CTCTGTAGAT ACCCATTCAC ACAATATCTG CAGCATAAGT TCTTAATCAA 1260 GACCAACTTC ACTCACTTTA ACTTCAAGAA CGTTGCAGGG GCCAGGCACT GTGGCTCACG 1320 CCTGTAATCC CAGTACTTTG GGAGGCCAAG GTGGGCAGAT 1360
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