Tag | Content |
---|
EnhancerAtlas ID | HS113-00414 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:17729050-17730460 |
Target genes | |
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 | CTGTGCCCTG GTGTGCCAGC TACCCCAGGA CATCTTACGA CATCTCGTTA ACCTGCCCAT 60 GGTGGTGCAG AGTTTATGGA CTACACTAGA GACCTCTTGT TGTATTCATG GCTCTGACCC 120 CTATACCAGC CTGGGACTGA CACAGACCAG GCCTTCAAAT ATGGGGAGGG ATGGATGAGC 180 TCATCTGCAT TTTCAGATAG TCTAGAAAAG CCAAAAGAAA TAGAGGACTC TGGACCCCAA 240 GGGCTTGGGG CTCCATCTCT AGGGAAAAAG GGGAGAGGAA AGCCCTAGGG CCAGAAGGGG 300 GACAAAAGGT TCACTCTTCC ACCCCCATGG GCTTTTCCCA GGGAACTTGC CCACCTCTAC 360 CAAGGGCTGC CTTAGGGTGG ATGAATTGGT CCCTCCTCTG ACCCTAACTA GACCCTCACC 420 CAGAGCTTTT CAGGTCAGCC CTGGGCCCCT CCCGCCCCAC CTGCCTAAGG GTCCTGCAGG 480 AAATCTTGGC AGCTTGACAC CCTTCTCTCC TGTTACCTCC CAGGCAGCAC CATCCTGATA 540 GCACCTGGAG AAGCACCCCC CCAGCCCTGG CTGTTAGCAG ACACCTGCAG CAGAGAGCTG 600 GGTGTACTTG GCTTGCACAG TGTTATAAAC GTCTCTAAGT TAGGCACTGA CAATTTACTC 660 AAAGTCTGGA TTTCCAGCTC CTGCTGCCAA GTCTTTAGAC CTGACCACAC TGGGCCCGAG 720 GCTGAAGACT CACTGGCCAC ACCCTCTAGA CAAAGATGTG CTCCAACAGG CCCCAGTCCC 780 CATCCCTCCC CACTGTGTTC CCCTGCAAAG GTCAGTGGTC ATTTGGCGCC ATGCTTGCAC 840 TACTGCTGTA GGGAAGGAGA GGAAATGCTC CCTGTACTGG CCAAAGGCAA GAAAACAAGG 900 TAAGTGGGCT CTGTGCCTCA GTTTCCTCAC CAGCGCAAGT GGGTAAGAGT TGTGCCTGTC 960 TCGAGGTTGT TCTGAGGACT GGAGTTATTT ACATAAAGCC CTAGAAAGAC ACGTGGCACC 1020 TCTCATTCCT GAAGGCTGGG AGACCACATC TCTGTAGAAG TAAACAAAAC CCTCCATTGC 1080 CTGCATAGCA GACACGGGGC CAGGCGCAGT GGCTCATGCC TGCAATCCCA GCACTTTGGG 1140 AGGCTGAGGC AGGTGGATCA TTTGAGGCCA GGGCTTCAAG GCCAGCCAGG CCAACATGGG 1200 GAAACCCCGT CTCTACTAAA AATGCAAAAA TTAGTCGGGG CATTGTGGCA TGCACCTGTA 1260 ATCCCAGCTA CTTGGGAGGC TGAGTGGCTG AGTTGAGAGA ATCACTTGAA CCCAGGAGGC 1320 AGAGGCTCCA AGATCATGCC ACCGCACTCC AGCCTGGGCA ACAGAGTGAG ACTTCGTCTC 1380 AAAAAAAAAA AGAACAAAAA TCACAGGAAA 1410
|