Tag | Content |
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EnhancerAtlas ID | HS052-02790 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:170379640-170380740 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr1:170379961-170379976 | TGCCCTCTGCCCTCT | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 170379973 | 170380371 | chr1 | 170379647 | 170379894 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I170409 | chr1 | 170378987 | 170380770 |
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Enhancer Sequence | ACTGCATTCT GAAATTAGCT AAGACTTTAG TCAAGTACTT TCCCACCAGG GAAAAGACAG 60 GAATTAAACT GAGACCTTAC GCATTCAAAT AAATGTTCGC AAGAGCTAAG GAATGCTTGG 120 TGTGTTCACA ACTAGTAAAA ATAACCTAGG GTGAAGAAAG ATGACTGAGT CATCTCATAT 180 TCCAGACCCA CTTTTTAAAA ATCCTAACTT GAAGGTCAAA AAAGTTCAGT AAACTTCTCA 240 TTTCTATTTT TTTCTCCTCC TCTTTCTTCC TTTCTTTGTT GCTTTCTTTC TTTTCTTTTT 300 CTTTTTTTTT TTTTTGTACT GTGCCCTCTG CCCTCTGCAA TTCTTGGCTC TTACAAGAGT 360 AGGGGAAAAA CTGCCTAAAT ATCATGAGAT AGGTGGCCCT CAGGGGTACT TCTTGTCAAG 420 CAGGAAGTGC CAAAGATCTT GTAAAATGTC CAATACAAAT TTTATTTTGC AGACTCTAGA 480 GGTTTGCATC TGGATACACA TCTGCATTTT CTGGGTGCTG GGCCAAACTG AAACATTCAG 540 TTTATCCATT GCTAATAAAC ATGTCAGCAG TTTCTTTGCT CTCACATCTG TTGTGAAAAA 600 TGTTATCTTT CCTGAAGTAT ATTTATTTTG TCTTTAATAC CAGCTTTCAT GGATTACAAA 660 CTCAAGATAT GCCTTCAGTT AACAAATTCA AAAGCATATG CTGGAAGGTG CCTCACTAGA 720 GTGATGAGAT AAATTAAAGA TGTATATTAT ATCTTAGATT CTGAAGAGGA AATCAGTGTA 780 AGGAATAACG ATGACTCTCA GGAAGGTTAT GTCAATTGAA ACAAGTTGCC TGTTAATCAA 840 GTTCATCTCA AAATCTATTC AAGGTACTCT ATGCATCACA GCAATTCGAC AAAATGTTTT 900 AAAAATTTAT CAGTTGTTTC ATTATTAAGG CTGTCTTCAG TCAAGCAGAT GACTTCCTTT 960 CCTAAGGAAA CCACCCCCAG GTACTTGCTT CTCCTTCTAT ATTCTCTAGA ATACTTGCTT 1020 TACCCAACTC ACTGATAGTG GGGCTATTAG AGAATCAAAT GAGGTTTTGC TTATTCAGAT 1080 GTCTGAAAAA GAAAACTGTA 1100
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