| Tag | Content |
|---|
EnhancerAtlas ID | HS105-02653 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr1:46985500-46986950 | 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 | CTCTTGACCT CAGGTGATCC ACCTGCCTTT GCTTCCCAAA GTGCTGGGAT TACAGGCGTG 60
AGCCACCGCC TGGCTGAGCC ATGGCGCCCG GTAGTTCCCC CTTCTCTTAG GCCTTGGCCA 120
ATGTTCTTGC AGCTCAGGGG TCTGGTTCCT TAGGGGCCCT CAGGGAAGGG GCCCCTGCTG 180
AGAGGGTCTG GGGAATGGAC CCCTTTAGGG CTGGGCACTT CCCTCATCTC TTTCCCACAG 240
AGCTGCTCTG GGCTGGAGCC CTCCACCCCC ATCACTCATT CTCCTTTAGC TTCTGGGAAA 300
GCCGATTAGG AGGTGGCCTT CTACCCGCCC CCCTGACAAG TGTGTCTGAA CTTCCAACAA 360
AGGCCCTCAG AGGGTTGCAG AGGGAGGGCT CAGCACTGGG AACCTGACAC CACTGGCCAG 420
GGATCACCCC AGCAGCCTAG GAGGCAGCTC TGTGGGGCTG CCCACCCCAC GGCAGGCAGG 480
AATGTCGCTC TGAGAGGGGA CCTGGTCCCA CAAAGGCCTG GGGGCTGGGC TGAGGCAGGC 540
TGGAGAGGTC TTCACCTGGG AGGCCTCACA ATAAGGAAGA CAGCAAGGGC CAGCACCCAG 600
GAAGGCACGT GGGAATAGGC ATACACGCCC CCACACACTG ACAGCCTCTC ACACACATTC 660
CCCATACATT CACAGCACAC ACGCACACAC GCATCCTCTC ACACCCCTGG GACATGTTGA 720
CTTCTGCACT GGACCACACA ATCCCAGGGT GTCTGTCTCC CTGTCTCTCA TGCCTGTGTA 780
CACAGCCCCA CTGCAAACCG GCAGACACAC AGCCACGCTC TGTCGCCTGA TGCTCCACAC 840
ACCCGCTCCA CCCCCAGACA TGCATTCTTC CCGGCTTGCT CACACTCCAG ACAGCCCCTG 900
AATGCTCAGT GGCACCAGCT CCCCTGTACA GACAGCCTCT CGAGCCAAAC TGCTGGCCTG 960
GTGCCCACAG AGACTTGGTG GCGGCTGCCC TGTGATTGTG GAAGATGCCA CCCAAATGCC 1020
CACATAAGAG TCAGACACTG GTCCCAGCTG CCATGTGAAC ACCCATGTGC ACCAACCCAC 1080
ACATCCACCC CAAGGGGCTG CCTTGAGCCC ACCTCTTCAC AGCATGCTCC CTCCTGCAGC 1140
AGCCTCATGG GCGTGTGACC CATGCAGTCA CACAGGGCCC TGGGCTCAGA GGGCCCGCAA 1200
TGTTCTGATG TCACCATCTT GAAATCTTTA CATTTTAAGC AAGGGGCCCT GCATTTTCAT 1260
TTTGCCCTGG ACCCCATAAA ATATATAGCT GGTCTCACTC CCACCCCATT TCTATTTATT 1320
TATGTATTTA TTTGAGACAG AGTTTTGCAT TTGTTGCCCA GGCTGGAATG AAATGGTGTG 1380
ATCTTAGCTC ACTGCAACCT CTGCCTCCTA GGTTCAAGCA ATTCTCCTGC CTCAGCCTCC 1440
CAAGCAGCTG 1450
|
| |
|
|
|
