| Tag | Content |
|---|
EnhancerAtlas ID | HS052-01242 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:46985620-46986800 | 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 | ATGTTCTTGC AGCTCAGGGG TCTGGTTCCT TAGGGGCCCT CAGGGAAGGG GCCCCTGCTG 60
AGAGGGTCTG GGGAATGGAC CCCTTTAGGG CTGGGCACTT CCCTCATCTC TTTCCCACAG 120
AGCTGCTCTG GGCTGGAGCC CTCCACCCCC ATCACTCATT CTCCTTTAGC TTCTGGGAAA 180
GCCGATTAGG AGGTGGCCTT CTACCCGCCC CCCTGACAAG TGTGTCTGAA CTTCCAACAA 240
AGGCCCTCAG AGGGTTGCAG AGGGAGGGCT CAGCACTGGG AACCTGACAC CACTGGCCAG 300
GGATCACCCC AGCAGCCTAG GAGGCAGCTC TGTGGGGCTG CCCACCCCAC GGCAGGCAGG 360
AATGTCGCTC TGAGAGGGGA CCTGGTCCCA CAAAGGCCTG GGGGCTGGGC TGAGGCAGGC 420
TGGAGAGGTC TTCACCTGGG AGGCCTCACA ATAAGGAAGA CAGCAAGGGC CAGCACCCAG 480
GAAGGCACGT GGGAATAGGC ATACACGCCC CCACACACTG ACAGCCTCTC ACACACATTC 540
CCCATACATT CACAGCACAC ACGCACACAC GCATCCTCTC ACACCCCTGG GACATGTTGA 600
CTTCTGCACT GGACCACACA ATCCCAGGGT GTCTGTCTCC CTGTCTCTCA TGCCTGTGTA 660
CACAGCCCCA CTGCAAACCG GCAGACACAC AGCCACGCTC TGTCGCCTGA TGCTCCACAC 720
ACCCGCTCCA CCCCCAGACA TGCATTCTTC CCGGCTTGCT CACACTCCAG ACAGCCCCTG 780
AATGCTCAGT GGCACCAGCT CCCCTGTACA GACAGCCTCT CGAGCCAAAC TGCTGGCCTG 840
GTGCCCACAG AGACTTGGTG GCGGCTGCCC TGTGATTGTG GAAGATGCCA CCCAAATGCC 900
CACATAAGAG TCAGACACTG GTCCCAGCTG CCATGTGAAC ACCCATGTGC ACCAACCCAC 960
ACATCCACCC CAAGGGGCTG CCTTGAGCCC ACCTCTTCAC AGCATGCTCC CTCCTGCAGC 1020
AGCCTCATGG GCGTGTGACC CATGCAGTCA CACAGGGCCC TGGGCTCAGA GGGCCCGCAA 1080
TGTTCTGATG TCACCATCTT GAAATCTTTA CATTTTAAGC AAGGGGCCCT GCATTTTCAT 1140
TTTGCCCTGG ACCCCATAAA ATATATAGCT GGTCTCACTC 1180
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