| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05356 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:35990830-35992000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr11:35991559-35991570 | CTTCTGGGAAA | + | 6.62 | | ZBTB18 | MA0698.1 | chr11:35991249-35991262 | CAGCCAGATGTTG | + | 6.25 |
|
| | 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 |
| GH11I035969 | chr11 | 35990653 | 35991470 |
|
Enhancer Sequence | CCAAGAACAG ATTTCAGATT TTCAGCCATT TTCCTCTTTT AATGGAAGCT CTGACTGGCT 60
AGTTGGTTAA TGGGTCCCAG GTTCTCCCAA GCCACTTAAC TTCCTAATTT TCAAGCATTA 120
TCCATGGAGA AAATCCACTC TGCAGAAGCT TATGACTTAA TGAGCTCAGT CAAAGTCAAT 180
CTGAAGTTGC AGGCAGCAGC TTTGATCATT GTGATAGGCG TTTTGGTTTC CACCGAGCAG 240
AGAATGGGAA AAAGCTTTGC CCATGATTTA TTAATCACTT CCTTGGCTGA GCTTTCTTGC 300
CTGGCTCTCC TGGGAAGCAC CAGTGTTGAG GTTGCTCAGG GTTCAGCCTC AGCATGGGCT 360
TTAGGTGTCC ATAGGCCCCG TGTTGCCTTG TTTCTGGAAG GCTTTGCTGA GCTGGAATGC 420
AGCCAGATGT TGGAACCAGA GGTGCACACC TTGAGTAAAC TCCTCTCTGC TTTCAAGCAG 480
CCCTTGAGGC CCCTTATTGG CAGAACCAGC TCCTCCAGGG AGGAGGCATG TGGGGCCCAC 540
GTGCATGCGT GGAGTTTTTT TCAGAGACCC ACTGATAAAA TATTTACTTC AGTGACATGG 600
TACCAAGTCC TGCTTTGTTT ATTTTAAAAG TCTTAATACA GCATTAGCCA TGAGGATACC 660
GGCTTATTTG CTTTTGGTTT CTTGCTTGTG GTTTTTGTTT TTATGAGGAG CAAAGAAGCT 720
AGGCCTGATC TTCTGGGAAA GTAGCCTGCT GTATGTTAGC CACACACTGG AAGAGGAAAA 780
CTGTTCTGTG TGGAGTGCTT ACTGTGTGCT CCGGGTACTG TCCTTAGTGC TTTTAGGTCA 840
TTATTTAATC CTCTCACAAT CATTCAAGTA GGTGTCACAG GTTAAATTGT GTCCCCTGAA 900
AAGGTACACT GAAGCCCTAA AACCTGGTAC TTGTGAATGC AAACCAATTT GCAAATGGGG 960
TCTTGACATA TGTAATTCGT TAAGACACAG TTCTGTTGGA CTGGAGTGGG CCCTAATTCC 1020
CATGACTGGT GTCTTTGTAA TAAGAGGGGG TACACAGACA CTCACAGAGG GAAGATGGCC 1080
TTGTGAAGAC AGAGGCAGAC ACTGGAGCAT GTAGGTGCAG GGCAAGGAAT GCCAAGGATT 1140
GCCAGCAACC TCCAGAAGCC AGGCAAGGAA 1170
|
