Tag | Content |
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EnhancerAtlas ID | HS053-00484 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:17786070-17787700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:17786610-17786625 | TGAACTCCTGACCTC | - | 6.22 | Zfx | MA0146.2 | chr1:17786635-17786649 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH01I017459 | chr1 | 17786481 | 17787685 |
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Enhancer Sequence | GCAACTGAGC AAGACTCCAT CTCAGAAAGA AAAAAAAAAG TTTTGATTCC CTATCACATG 60 CTTCATAAAT TACAATGTCA TGAAATCTTC ATAACAGCCA AGTCTGGGTA ATGGGTATAA 120 TACCTTGGGG CAGGTATTAT TATTGTTATC ATAGCTTTTT TTTTTTTTTT TGAGGTGGAG 180 TTTCACTCTT GTCTCCCAGG CTGGAGGCTG GAGTGCAATG GCGTAATCTC GGCTCACGGC 240 AACCTCTGCC TCCCGGGTTC ACACTATTCT CCTGCCTCAG CCTCCCAAGT TGCTGGGATT 300 ACAGGCGTGG GTCACCATGC CTGGCTAATT TTTATTTTTC CGAGACAGTC TCGCTCTGTC 360 GCCCAGGCTG GAGTGCAATG GTGCGATCTC AGCTCACTGC AACCTCCACC TCCCAGGTTC 420 AAGAGATTCT CCTGCCTCAG CCTCCCCAGT AGCTGGGACC ACAGGTGTGC GCCACCACGC 480 CCAGCTACTT TTTGTATTTT TAGTAGAGAT GGGGTTTCAC CATGTTGACC AGGCTGGTCT 540 TGAACTCCTG ACCTCAGGTG ATCCACCCGC CTCGGCCTCC CAAAGTGCTG GGCTGATAGG 600 TGTGAGCCAC TCTGCCCGGC CTGTTTTTAC CATTGCTATT TTATACGTGC TCAGAGAGAT 660 GACCTAAGTT CCCAGAAGTG ACACACGGGA AAGCGGCAGA GCTGGATTCA ACCCAGGCTT 720 GTGGAATCCC AGAGCCTATG CCCTTCCCTT CGCTGTGTCA CATCTTCCTC TAAGGACCCA 780 GTGAAACCCA AGTTCTCTGG GTGTGATTCA CTCCCTGGAG TCCTCCGCCA TCCAGAGGGT 840 GGGTTCCGGA GTTGCCTCCT TCTCTGCATC CCAATTGGAT TCCTCAGAGC CACCGCCTTC 900 CTCCTGCCCA GCTCAGTGCA GGGTGCTCCG GCGCCTGGCA TCTGAAGGAT GTGCAGGCAG 960 TGGCGTGATA GTGAGTGGGA GGAGGAGCCT CTGATCATCC ACCAAGTTCA AACCTGCTTT 1020 TCCTGGCATG ACCCTCAGCT AGGCAGCCCG GACTCTCCAG ATGCCAGCCT GGCCATGCCA 1080 GGGGCCAAGG AGGATGCTTC AGGCAAAATC CCCACATGCA AGATGCTGGC TTCCCAGGGC 1140 TCCTCCAGGG TGGCAGGTGA CAGGCATGTA CGCTAGGGAG GGGACATCGG AGCTCTTCAG 1200 CCAAGCAACT CTGTTCGGAG AAAAAAGAAA AACCTTCAAG TCCTCGGGAG TGCCTCAAAG 1260 CAGAAACCTC AACCTGAAAT ACAGACCTCA TTCAACCTGG CCGTGAATCC TTGCCACACC 1320 TTGCATTAGA GAAAGGCTCC TTTCCAAACC ATTTCATGTG TGTGTTAAAA ACCATTTCTG 1380 GGCGGGGCGC GGTGGCTCAC GCCGGATCGC CTGAGGTCGG GAGTTCCAGA CCAGCCTGGT 1440 CAGCATGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAT TAGCTGGGCG TGGTGGCAGG 1500 TGCCTATAAT CCCAGCTACT CAGGAAGCTG AGGCAGGAGA GTCGCTTGAA CCCTGGAGGT 1560 GGAGATTGCA GTGAGCCGAG ATCGCGCCAC TGCACTCCAG CCTGGGTGAC AACAGAGTGA 1620 GACTCCATCT 1630
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