Tag | Content |
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EnhancerAtlas ID | HS145-09532 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr16:88973750-88974650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr16:88974526-88974536 | ACCACTTGAG | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr16:88974533-88974548 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 88973853 | 88973989 | chr16 | 88974392 | 88974534 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I088907 | chr16 | 88974381 | 88974450 |
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Enhancer Sequence | CAGAACAGCA CTGAGGTCCT CCTGCTGGGG TGGGTGGGGT CAGTCTGGGT CCCAGTCCCT 60 TCCCTATGGC CCTGGCTCAG AGGCAGGTGG GCAGCGGGTG CGGAATCTGA CGAGAAGGGC 120 TCTGACGCCC GGAGGGGAGG AATCTCATAC AGAGGACCAA CTCTGTCCTC ACGGATTCTT 180 CCGCGGCCCT GAGATCCTGC GCTTCTCTAT CTTACGAGTG GGGAAACAGA GGCACAGAGA 240 GGCTGAGGAG GGGGAGAGCC AGGTGTGGAT CCAGGTGACC TGGCCCAGCT ACCCCTTCCC 300 CACTGGCCAC AGAGGGCACC TGCAGCCTGG GAACCCCGAG GGGAGGCACC TGCCCTCCTG 360 GCCTCCCTCT GTGGCTTGGG CCTCTGCCAA GTGTCCTTCT CACTCCCCCT GCCCATGACT 420 GACGGTGGCA TCTTCTAATT GTCCCCTCAC CCCAGAGCAG GGGCTTTGCC TGTCCTTCCC 480 ACCCTCGATG GCTCAGGCAC TGGCTCTGGA CACAGTGCGC CCCTCTCTGG GCATGCCTGA 540 GTCTGCCCTG ATGTTGGGTT TCCCTCTATG CGGTTTTCCC CAAAGGGTCT GGGCATGCAG 600 GAACTGGTCA GATGTCTAAA GGAAGAGGAC AGGGAGAGAG TGCCAGTTCC TCCCCCAGCC 660 CTGGCTGCAG CCTCATCTGC CTCCCAAGCT CCCACTCATC AAGAAAGTTC CCAGACCTGC 720 CAGACGTGGT GACTCACACC TGTCATCCCA GCACTTTGGG AGGCCAAGGT AGGCAAACCA 780 CTTGAGGTCA GGAGTTCAGG ATCAGCCTGG CCAACATGGT GAAACCCCGT CTCTACTAAA 840 AATGCAAAAA TTAGCCGAGC GTAGTGGTGC GTGCCTATAA TCCCAGCTAC TTAGGAGGCT 900
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