Tag | Content |
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EnhancerAtlas ID | HS147-14099 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr14:81832290-81833650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr14:81833269-81833280 | ACAGATAAGAA | - | 6.14 | Gata1 | MA0035.3 | chr14:81833269-81833280 | ACAGATAAGAA | - | 6.62 | ZIC3 | MA0697.1 | chr14:81832906-81832921 | GCACGGCAGGGGGTG | - | 6.17 |
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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 |
GH14I081366 | chr14 | 81832741 | 81832890 |
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Enhancer Sequence | CTACCCTGAC TGGTGAAAAT AGCAGGGTGT GCCCACCTTG TCTAGACAAA GGAGACTCCT 60 GTGGAGATGA GGGGTAAGAG AGGAGTGAAA TGTTGTTTGG GATTTTGCCT ATTAACAATT 120 CTCCTGCCAT TCGCTCTTGA GAGCAGACCT CAGAGCTAAC ATCAACACTG CTCTCCAGCT 180 CTGCCCCCCC GCACCCTGTG ATTTAACCAA GGTAAGGGGA TTTGTTTGCC TTCCTACTAA 240 TTATCCCCTT GGTGAGAAAA TGAGAATAAA GTGTAGGCTG ATCACAGAGT CTTTCCCTCC 300 ACGATTATGC TGGGAACTGG ATTGCCCTGC AGGGCTGCCA AATCCCTGCA GAACTCTGCC 360 GCAGATGACA GGGAAGAGGC TGTGGCTCTG CTCTCGGCAG CCCACTACCA AGCAAGGGGG 420 CCAAGGCAAA TAGGCTGGGC CCAGAGCACC GTAATCCCTC TCCAAACAAG AGATGAATCA 480 CAGAACATGA GGTGCCCAGT GGTTACCCTG ACACACTGTG CTGCCAGGGA GAGCCCAGCT 540 CAGCTGAGGG AGCTCCGGAT GAGACTGCAG TTCCAAGGAA CTCTTCAACC TCTACCACCC 600 TCTGCAATGC TAAAGGGCAC GGCAGGGGGT GGGGGGGCAA TGACAAACAT CTCCCCAAGG 660 CAGTTCCTCC CAAGGTTCCC CAGGCACAGA AACCAATCAT ACCGAACTCC CCACTGCATC 720 TCTGTATTTA CTGCTTGCTG CTGAGAAATG CAAAGCACTT CTCAGATCTC ATTCCACATG 780 CTATAGTTTG AGTAACAGCT TTCTTTGGGG GTAACAGAGG AGTCGACAGT AATTATCCTT 840 ATGCCCCATA TCAAATGGAA ATGAGGCAGA GAGATATTAA ATTAAGATTT TTTTTATTCC 900 TACAGCACTT GGCACTGTAC GAAACACCTT CATATATACC CTGTCACCCT GACTGAGCAG 960 GATCGCTCAG TTCCATTTTA CAGATAAGAA AGTAAAGCTC TGAAGAAATG ACTTACCCGG 1020 AGGACAGACT GATGGGAATC TGCCCCATAA CCCCAGGGGG TTTCGGTTTA CCCAACTGGA 1080 ACCATCCAGC CTCAAAGCAG GGCTCTCCCA GAGGTTGGCA CTGCCACAAG CCTGGTGCCA 1140 GGCAGAGGGC AGGGCATCAC CTGGCTGGAG GGCTTTCCAA TGTGTACAGA TATCCTTGAA 1200 GCTCTCGATA GCTCATCTGA AAGCATTTTT TTCTTCCTTT TTTTTTTTGT GAGACCAAGT 1260 CTCACTCTGT CAGCCAGGCT GGAGTGCGGT GGCACGATCT TGGCTCACTG CAGCCTCCGC 1320 CTCCTGGGTT CAAGCAATTC TCCTGCCTCA GCTTCTCAAG 1360
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