Tag | Content |
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EnhancerAtlas ID | HS098-52835 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr7:101331310-101332280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6 | MA0677.1 | chr7:101331523-101331537 | CAGGTCCAAGGTCA | + | 6.02 | Nr5a2 | MA0505.1 | chr7:101331524-101331539 | AGGTCCAAGGTCAGG | + | 6.25 | Nr5a2 | MA0505.1 | chr7:101331512-101331527 | GGGGTCAAGGTCAGG | + | 6.54 | ZNF263 | MA0528.1 | chr7:101331416-101331437 | CCCTCCTCTCTTGCCTCCCCC | - | 7.11 |
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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 |
GH07I101688 | chr7 | 101331305 | 101332280 |
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Enhancer Sequence | CTGTCCCCTG TCCCTCCCAG TGCACCCTGA GCCCACCCTA CCCAGCCCCC GCCACCCCCC 60 TGCTGCACTC CCAGGGCTGA CCTTCTTCCC TGCCCAGGCT GGACATCCCT CCTCTCTTGC 120 CTCCCCCTTG ACCTCCCTGA TGGGACTAAG TGGAGGCTTC TGTTCATGGA AACTGGGGTT 180 AAGGAAGCAA ACTACAGGGC CTGGGGTCAA GGTCAGGTCC AAGGTCAGGG CTGAGTCAGC 240 CCTGACTTCG TTCCTCCCGC CTCTTCCCCC GGGCATCCAG GCCCTTAGGT GTCAGGAGTT 300 ACAGCCTTGC CCTCGCCTCC TGCTCCTCTG GCCGAGGCCA GGGCGGCCCC TTCCTGTCCC 360 CCCTGCCCGT CGTTCGCTCC CCGAGGGCGC AGCAGAAGCA CGGGGAACTC CGGACCCCAC 420 GAGGCGCTCT GGACGAGGTC GAGCCGCCGC TTCCCCCGGG CGCCGCTAGG TGGCGCCGCG 480 CTAACGAGGA TCGGGATAGA CCGGAGGGGC CGCGCTGCCA CCAACCGGGT CTCCACTCCC 540 CAGGTCCTCA CTCCCCGGGC CCCAGCCTCG CCCCAAAGCT CAAACACGCA CCCGGGAACC 600 CTTCCACCAC CCTCCCTCCC CACCCCTGGC ATCCTTAGCC CTCGGCAGCT CCCGTGGTCC 660 CAGGGGCCTC TCCGGTCCCT CAGCAGGAGA CCTGGAGTGC ACGGCCTGTC CATGCCTCTG 720 GGACGCAGGA CAAAGTGGAC GAATAGGAAT CAACCGTGGG GAGGGAGGGG CCACCCAGGA 780 GAATCCCAGT CCACGGAGTA AGGGAGGGTG GCATGCTGAG TGCCAGGCAG AAGGCCTGGC 840 CCAGGCGGTG CTCCCTAAGT GAGGGTGCAC CCTCACTTAC ATCCTTCCAG GATAGTTCCT 900 CTTCACATCC TTCCAGGATA GTTCCTCGCC TAGGCGTTTT CTCCCTCAGT TTGGGGGTAG 960 TGGTTTTTAG 970
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