Tag | Content |
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EnhancerAtlas ID | HS103-00556 | Organism | Homo sapiens | Tissue/cell | HUES64 | Coordinate | chr1:46985290-46986780 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr1:46985789-46985800 | CTTCTGGGAAA | + | 6.62 |
| | 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 |
GH01I046519 | chr1 | 46985499 | 46989059 |
| Enhancer Sequence | TTTTGAGATG GAGTTTTGCT CTTGTTGCCC AGGCTGGAGT GCAATGGTGC GGTCTTGGCT 60 CACTGCAACC TCCACCTCCC GGGTTCAAGG GATTCTCCTG CCTCAGCCTC CCCAGTTGCT 120 GGGACTACAG GCGCTGACCA CCACTCCTGG CTAATTTTTT GTATTTTTAG TAGAGACGGG 180 TTTCACCATG TTGGCCAGGC TGGTCTCAGA CTCTTGACCT CAGGTGATCC ACCTGCCTTT 240 GCTTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGCC TGGCTGAGCC ATGGCGCCCG 300 GTAGTTCCCC CTTCTCTTAG GCCTTGGCCA ATGTTCTTGC AGCTCAGGGG TCTGGTTCCT 360 TAGGGGCCCT CAGGGAAGGG GCCCCTGCTG AGAGGGTCTG GGGAATGGAC CCCTTTAGGG 420 CTGGGCACTT CCCTCATCTC TTTCCCACAG AGCTGCTCTG GGCTGGAGCC CTCCACCCCC 480 ATCACTCATT CTCCTTTAGC TTCTGGGAAA GCCGATTAGG AGGTGGCCTT CTACCCGCCC 540 CCCTGACAAG TGTGTCTGAA CTTCCAACAA AGGCCCTCAG AGGGTTGCAG AGGGAGGGCT 600 CAGCACTGGG AACCTGACAC CACTGGCCAG GGATCACCCC AGCAGCCTAG GAGGCAGCTC 660 TGTGGGGCTG CCCACCCCAC GGCAGGCAGG AATGTCGCTC TGAGAGGGGA CCTGGTCCCA 720 CAAAGGCCTG GGGGCTGGGC TGAGGCAGGC TGGAGAGGTC TTCACCTGGG AGGCCTCACA 780 ATAAGGAAGA CAGCAAGGGC CAGCACCCAG GAAGGCACGT GGGAATAGGC ATACACGCCC 840 CCACACACTG ACAGCCTCTC ACACACATTC CCCATACATT CACAGCACAC ACGCACACAC 900 GCATCCTCTC ACACCCCTGG GACATGTTGA CTTCTGCACT GGACCACACA ATCCCAGGGT 960 GTCTGTCTCC CTGTCTCTCA TGCCTGTGTA CACAGCCCCA CTGCAAACCG GCAGACACAC 1020 AGCCACGCTC TGTCGCCTGA TGCTCCACAC ACCCGCTCCA CCCCCAGACA TGCATTCTTC 1080 CCGGCTTGCT CACACTCCAG ACAGCCCCTG AATGCTCAGT GGCACCAGCT CCCCTGTACA 1140 GACAGCCTCT CGAGCCAAAC TGCTGGCCTG GTGCCCACAG AGACTTGGTG GCGGCTGCCC 1200 TGTGATTGTG GAAGATGCCA CCCAAATGCC CACATAAGAG TCAGACACTG GTCCCAGCTG 1260 CCATGTGAAC ACCCATGTGC ACCAACCCAC ACATCCACCC CAAGGGGCTG CCTTGAGCCC 1320 ACCTCTTCAC AGCATGCTCC CTCCTGCAGC AGCCTCATGG GCGTGTGACC CATGCAGTCA 1380 CACAGGGCCC TGGGCTCAGA GGGCCCGCAA TGTTCTGATG TCACCATCTT GAAATCTTTA 1440 CATTTTAAGC AAGGGGCCCT GCATTTTCAT TTTGCCCTGG ACCCCATAAA 1490
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