Tag | Content |
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EnhancerAtlas ID | HS095-00392 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr1:17729240-17730310 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr1:17730107-17730118 | AAGTAAACAAA | + | 6.62 | KLF4 | MA0039.3 | chr1:17729786-17729797 | CCACACCCTCT | + | 6.02 | Klf1 | MA0493.1 | chr1:17729784-17729795 | GGCCACACCCT | + | 6.32 | Nr5a2 | MA0505.1 | chr1:17730221-17730236 | GGCTTCAAGGCCAGC | + | 6.04 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTCAGATAG TCTAGAAAAG CCAAAAGAAA TAGAGGACTC TGGACCCCAA GGGCTTGGGG 60 CTCCATCTCT AGGGAAAAAG GGGAGAGGAA AGCCCTAGGG CCAGAAGGGG GACAAAAGGT 120 TCACTCTTCC ACCCCCATGG GCTTTTCCCA GGGAACTTGC CCACCTCTAC CAAGGGCTGC 180 CTTAGGGTGG ATGAATTGGT CCCTCCTCTG ACCCTAACTA GACCCTCACC CAGAGCTTTT 240 CAGGTCAGCC CTGGGCCCCT CCCGCCCCAC CTGCCTAAGG GTCCTGCAGG AAATCTTGGC 300 AGCTTGACAC CCTTCTCTCC TGTTACCTCC CAGGCAGCAC CATCCTGATA GCACCTGGAG 360 AAGCACCCCC CCAGCCCTGG CTGTTAGCAG ACACCTGCAG CAGAGAGCTG GGTGTACTTG 420 GCTTGCACAG TGTTATAAAC GTCTCTAAGT TAGGCACTGA CAATTTACTC AAAGTCTGGA 480 TTTCCAGCTC CTGCTGCCAA GTCTTTAGAC CTGACCACAC TGGGCCCGAG GCTGAAGACT 540 CACTGGCCAC ACCCTCTAGA CAAAGATGTG CTCCAACAGG CCCCAGTCCC CATCCCTCCC 600 CACTGTGTTC CCCTGCAAAG GTCAGTGGTC ATTTGGCGCC ATGCTTGCAC TACTGCTGTA 660 GGGAAGGAGA GGAAATGCTC CCTGTACTGG CCAAAGGCAA GAAAACAAGG TAAGTGGGCT 720 CTGTGCCTCA GTTTCCTCAC CAGCGCAAGT GGGTAAGAGT TGTGCCTGTC TCGAGGTTGT 780 TCTGAGGACT GGAGTTATTT ACATAAAGCC CTAGAAAGAC ACGTGGCACC TCTCATTCCT 840 GAAGGCTGGG AGACCACATC TCTGTAGAAG TAAACAAAAC CCTCCATTGC CTGCATAGCA 900 GACACGGGGC CAGGCGCAGT GGCTCATGCC TGCAATCCCA GCACTTTGGG AGGCTGAGGC 960 AGGTGGATCA TTTGAGGCCA GGGCTTCAAG GCCAGCCAGG CCAACATGGG GAAACCCCGT 1020 CTCTACTAAA AATGCAAAAA TTAGTCGGGG CATTGTGGCA TGCACCTGTA 1070
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