Tag | Content |
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EnhancerAtlas ID | HS052-13354 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr15:76462210-76463330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2F1 | MA0017.2 | chr15:76462326-76462339 | CACTTGACCTCTG | - | 6.62 | RREB1 | MA0073.1 | chr15:76462594-76462614 | CGGGTGGGTGTGGTGGGTGG | - | 6.49 |
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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 |
GH15I076170 | chr15 | 76462021 | 76463154 |
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Enhancer Sequence | GAGGTAAAGA CCAATGTCCA CCCCCAAAGC CCCCACTCTG CCATCCTGGA AGCTGGAAAA 60 CGTCATGTCC CATCCATTCC AGGGTGGACA CCATCAAGAA GGCTGGTTCC TTCTCCCACT 120 TGACCTCTGT GGCTGTGCAT GTTGGGTGGG GCAGGGAGGG GGAACTGAGA CTGTTTCCAG 180 CAAAGGAATG TTCTGAAACA TTCATTTAGA ATGTTAAAAG GAATGCAGAA CTCCTTGAAG 240 TTCTGCAAAA TTTTACAATT TGAATCAATT TGAAAAGCTT TTGAAATGTG TTTTAAAACA 300 AATAAATCCA CCCTAAATGG AAAGCTGAGC GGGAAACTGT CAACGTGCTT CTCAGGCTGG 360 GTTTCCGTTC TGCTTCCCGC CACACGGGTG GGTGTGGTGG GTGGGATGAG GTCAGGGAGG 420 CCTGGCTGTC GCTGGCAGTG TTGTGCACAC AGACAAGGCA AGGCGGCCAG ATCTGCTGCC 480 CACTCCTTCC TCACCTCTCC ATCTATATTT CAGCCTCTTT GGCTCAGTGC TGGGATCTGA 540 CACAGTGCTG GGATCTGACA CAGTGGGCCT GGCCGATGGA TGGCTCAGAA CACGGCCAGG 600 CTGGGGCAGG CGGACGGAAG GGCAGGGCCC AGGGCTTCAT TGTGCAGGCT GGGCCCACTT 660 CTCACCTAGC CCTGCCCCGC TGGAGAGTTA GAGACTCTGC ACTGGACACA GCTGAGATGC 720 GGGTTCCGGG CTCCTGTTCC CCTCGGGGAA GGAGGCACCC TGAGCCTGCC TTCAGCCCCT 780 GCCCTGCCAG GGAGGGATCC AGCTTGGCCT CTGCCCAGGG CCTGGGATAC AGGATGCAGG 840 CCCTATCTTG AGAAGGGGCA AGACAGCCCA AGGCCATCTG AACTAAGGGC TGGAGATGGG 900 CTGAGGTCAC TTGGAGGACA GAGTGCATTC AGGAGAACGT CTAGGAGGAG GAGGCCCCTA 960 AAGACTCAGG AGGGTCAGGA GGGGCCACCC GGGGTGGGGT GGCCTTCTGG TGGGGGCCCG 1020 GGCTGCTGGA AAAGTTGGGC AGCACCAGCT GCTTTGCCTG ACTGACCCCT GGTCCCGGAC 1080 ACACGGCAGG GCCCAGGGCA CTGAAATGGG CCTCCTCTCA 1120
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