| Tag | Content |
|---|
EnhancerAtlas ID | HS045-01633 | Organism | Homo sapiens | Tissue/cell | Fetal_lung | Coordinate | chr1:46985540-46986730 | 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 | GTGCTGGGAT TACAGGCGTG AGCCACCGCC TGGCTGAGCC ATGGCGCCCG GTAGTTCCCC 60
CTTCTCTTAG GCCTTGGCCA ATGTTCTTGC AGCTCAGGGG TCTGGTTCCT TAGGGGCCCT 120
CAGGGAAGGG GCCCCTGCTG AGAGGGTCTG GGGAATGGAC CCCTTTAGGG CTGGGCACTT 180
CCCTCATCTC TTTCCCACAG AGCTGCTCTG GGCTGGAGCC CTCCACCCCC ATCACTCATT 240
CTCCTTTAGC TTCTGGGAAA GCCGATTAGG AGGTGGCCTT CTACCCGCCC CCCTGACAAG 300
TGTGTCTGAA CTTCCAACAA AGGCCCTCAG AGGGTTGCAG AGGGAGGGCT CAGCACTGGG 360
AACCTGACAC CACTGGCCAG GGATCACCCC AGCAGCCTAG GAGGCAGCTC TGTGGGGCTG 420
CCCACCCCAC GGCAGGCAGG AATGTCGCTC TGAGAGGGGA CCTGGTCCCA CAAAGGCCTG 480
GGGGCTGGGC TGAGGCAGGC TGGAGAGGTC TTCACCTGGG AGGCCTCACA ATAAGGAAGA 540
CAGCAAGGGC CAGCACCCAG GAAGGCACGT GGGAATAGGC ATACACGCCC CCACACACTG 600
ACAGCCTCTC ACACACATTC CCCATACATT CACAGCACAC ACGCACACAC GCATCCTCTC 660
ACACCCCTGG GACATGTTGA CTTCTGCACT GGACCACACA ATCCCAGGGT GTCTGTCTCC 720
CTGTCTCTCA TGCCTGTGTA CACAGCCCCA CTGCAAACCG GCAGACACAC AGCCACGCTC 780
TGTCGCCTGA TGCTCCACAC ACCCGCTCCA CCCCCAGACA TGCATTCTTC CCGGCTTGCT 840
CACACTCCAG ACAGCCCCTG AATGCTCAGT GGCACCAGCT CCCCTGTACA GACAGCCTCT 900
CGAGCCAAAC TGCTGGCCTG GTGCCCACAG AGACTTGGTG GCGGCTGCCC TGTGATTGTG 960
GAAGATGCCA CCCAAATGCC CACATAAGAG TCAGACACTG GTCCCAGCTG CCATGTGAAC 1020
ACCCATGTGC ACCAACCCAC ACATCCACCC CAAGGGGCTG CCTTGAGCCC ACCTCTTCAC 1080
AGCATGCTCC CTCCTGCAGC AGCCTCATGG GCGTGTGACC CATGCAGTCA CACAGGGCCC 1140
TGGGCTCAGA GGGCCCGCAA TGTTCTGATG TCACCATCTT GAAATCTTTA 1190
|
| |
|
|
|
