Tag | Content |
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EnhancerAtlas ID | HS179-05443 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr10:99522090-99523550 |
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) |
TEAD1 | MA0090.2 | chr10:99522803-99522813 | CACATTCCAT | + | 6.02 | ZNF263 | MA0528.1 | chr10:99522656-99522677 | GCCTCTCTCCTCTCCTCCCTC | - | 6.18 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_47588 | chr10:99521825-99522746 | Pancreas | SE_47588 | chr10:99522757-99523471 | Pancreas |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 99522981 | 99523438 | chr10 | 99522454 | 99523132 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I097762 | chr10 | 99521938 | 99525775 |
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Enhancer Sequence | CTCTGCCAAT CCTTTTTGTG GTTGGTTGTG TTGAGCAGCC TCCCGTGAGC CATGGCCGAC 60 CTTGAGCTGG CAGTGGTTTC TGGGATCTTC AGGATTTTCA GCCCTCGGGG CTGAAGCCAT 120 ATGAAGTTCT GTCTTCATCC CCTTGTCTCC CTGGAACCTT TGAGGCACCC CCTAAGAGAG 180 GCCCTGGCCC AGCATCTGTC TTACAGCTGG TGGCCCTCAG GATAACACCT ACATTGATGG 240 AGCACCTGTG CCAGGCACCA TGCTGAGTGC ATCATCTCAT CGAGACCTCA TGACAATCTC 300 CAAAAGTAGG TTCTGTTGTT AACTCTGTTT AACTGACGAG TAAAAGGAGG TGTGGGGAGG 360 TTAGGGAACC TGCCCAAGGT CACATAGCTA GTAAGTCGTG GAGCCGGGAT GTGAATTATG 420 CCACATGAGC TTGCAGGGGC CTCATAAGAG AACCTTTGGA GGAACAGAGC AATCCTGGGT 480 GCCACCCTCC CCCTCTTTCT GCCTGGCCCC CACTGGCTCC AGGAGCTAGC CACTGAGCTA 540 ACAAGAAGGC CTACCCACTA AGCATGGCCT CTCTCCTCTC CTCCCTCCCA CCCCCAGCCC 600 TAGCGAAATG GGCTCAGCCA CAAGAACAGA GGCAGCCTTG TGGCCGGAGC TCCCCCAGCT 660 CCCAGCAACC CCACCTCCGG CCTGGTCGGG TATGTTTCAA CACCCCAGAG CAGCACATTC 720 CATTCTCTGG CACAGCTGGG GGCTGGGGAT TCCGGATTCC CCTGGCTGCC TGTGTTCTTC 780 ACAGCCCCAG CAGAGCCTGC TGTCTGGGCT GGGACATGGG GTCCCAGCCA CACACATTCC 840 AGCAGCAACC ACCCCCCCAT GTTACATTTC CCCAGGAGTG AACTTCAGCC AGGATTACAG 900 GCGACTAAAC AGTTGTGGGA TGTGAGCTTC CTTTGTGGAG ACCTAAGGCT GGATGCTGGC 960 AGGGCTGAGA GGGGAGAAGG GGTTGGGGGT GGGCTGTCTT TGGGAATTAG GAGAAAAGCC 1020 ACTGGCTCCT CTGCCTCTGT CAGGACCCTT GGAGTGGGAT TGGAACAGGG CTCCCAGAAA 1080 TCTTCCTGTG AGGCAGGCTG GCAGAAGCAT GGCTGCCTGC ACCCCTGAGC CTTGGCTTTG 1140 CCCCTACCGA TAGTAGTATA GTGGTTAAGA GCATGAAGTC AAATTCTAGC ACTGCCATGT 1200 GCAAGCTGTG TGACCTCCAA CAAGTTCCTT AACCTCTTTG AGCCTCAGCC ACCATCACTG 1260 AAATGCCACT ACCTCAAATG GCTGTTGGGA GGCTTAAATT AGAATGCAAA AGCTGGGTGA 1320 GGCACAGTGG CTCATGCCTG TAATCCCAGC ACTTTGGGAG GACAAGGAGG GAGGATTGCT 1380 TGTGTCCAGG AGTTTGAGAG CAGCCTGGGC AACATAATGA GACTTCAACT CTAAGAAAAA 1440 TAAGAGATTA GCCGGGCATA 1460
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