Tag | Content |
---|
EnhancerAtlas ID | HS052-03037 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:183385580-183387310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:183385614-183385635 | CAAAGGAAAGTGAAAGTGGAG | - | 7.98 | IRF2 | MA0051.1 | chr1:183385618-183385636 | GGAAAGTGAAAGTGGAGT | + | 6.25 | ZNF263 | MA0528.1 | chr1:183386922-183386943 | TCTCCAGCCCCTTCCTCCCCT | - | 6.04 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I183416 | chr1 | 183386008 | 183386935 |
|
Enhancer Sequence | AGGAAAAGAA GGAAAGGGAT GAAGACACCA GCATCAAAGG AAAGTGAAAG TGGAGTGTTC 60 TTAGGGCACT GATAGTCCTT AGAAGACTGA TGACATGCTC TTGTCTACCC TGATGCTGGA 120 ACAGAAGTCC TTATTTAACA GGCAAGTTGG CATTGGTTCT TAATAAAAGA CTTTTGAAAG 180 CTGAAGGAAT GGTGAAGAAG GGATGGCTAT CTCTCAGCCT CCCTCCTTCT ATCGTGTAGA 240 TATGCCTACC CGATTTGCCC TTTGCTCAAA GTAGTTCTAT ATTCTTTCCA TGAGGTTTTT 300 AACAAGCGAG CCCAGTTCAG CGCACCTTTT AAGTTTAAAG ATGAATATTT TTAGCCTAAG 360 CCACCTCGCC CTGTCTTTAC CGCTGTGGTG TGGTTTTCAC TAAACCTCCC TAGGAGGGCT 420 CGCGCAGTCC TCAGGCTCCG GATAAACACG TGTGCCCGCA TCCAGCTCCG GCGCGCCCTG 480 CATTTCAGCA CCGCCGCCTC TGGAGAGCGC CTTGCTGGCG GGCCAGGTCA GGGCCTCCCA 540 CACGCTCTCT CATCCATCCC AGCCCACTCG CTTTTCCCTA CTCCTCGCTT CTCTCAGTTT 600 CAAGAAAAAG CACCCCCAAC TTCTAACTTC TCAATTCCTG CTTCTAAAGT GACCTCCGCG 660 TCCCTCTTTC CGTGTCTAAA CGCTCATGCC CCACGCCTTT GAGTCCTACG AGCAGCTGCG 720 AAGCCGCGTG GCTTCCCACC GGTGGCGCGA GACCTCCAAT AGGCATCTAT CGATCACCTT 780 TCCCCTACCG CTGCTGGACC CCGAACCAGC CAGCCGGATG CCCCCGCTCG CTCTCTCTGA 840 CTCCACGCCC CAAAGCTTCT AAGAAACAAA CGCGCGATAA GTCCCCTCCC CCCAACACGC 900 ACACGCATAT ACTCACACAC AGTCATTCGC ACATTCGTAC ACACACTAGA CGCCTCAAGC 960 CTTCCGAGTG CCATCGCCAC CCTGGGCAGA GCCTCAGCCA ACTTGGGCCC CGATCCTTCG 1020 GCTCCGGCTC GCGCAGGGCC TCCCGCAGCC TCCGCCCGGC CCCCTCCCCG TCCTAGGCAG 1080 CGGGTCCCTG AGGCCGAACC TAGGCGGAAA AGGGCCCCCT CCCTATTCAC TCAGCATCCA 1140 CCTCGCGCGG GCAATACACG GCCCACAATT CCCAAACACT GGTCCCTGGG CCGCCCAGAA 1200 TCACCAGCCA AATCCGAAAT TAATCTTGAA GCCCCAGCCC CTGTCACCGG TGTGTCGGGC 1260 GCGAGTGTGT TTGCGAATCC CAGGCACATA CATGATTTAA CTCCTTCGAG CTTTCGGCCC 1320 ATCCTAAACA AACAGCACGT TATCTCCAGC CCCTTCCTCC CCTACTCGGC GCCCCAACCT 1380 CTGCCCCCAT CCCGGTCTTC GCCAGCCTGG TAGCCGAACC ACCGCACCGC CACACTCCAG 1440 TTCTGGTATC TCGAACCCCT GCCCAGCCCC AAATGATACT CATCTCTAGT CCCCTCCCAT 1500 CCCCCACCTT TGGCCCCCTG CGAGCCGGGT CTGGCCCCGG CAAGTGACGC CTCGGAAACG 1560 CAGTCTGCGT ACCCTCCCCT GAGTCCAAAA TGAAGGGGCC GACCTCCACC AGCTGGATGA 1620 GCCGGCCCAC CCCTCCGAAG GGGCACACGC CTTCCCGTTC GATCGCCCTG GAAAACACAG 1680 GTGCCTGGGA AAGGAGAGGA GCGGAAGCGG CTTCCAGAGG TGGGCGGGAG 1730
|