| Tag | Content |
|---|
EnhancerAtlas ID | HS184-11080 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr15:42169560-42170530 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBXT | MA0009.2 | chr15:42169914-42169930 | TAACACCCTTGTGTGA | + | 6.13 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGGATGACAG GCAGAGAGTC AAACCCCAGC AGGCTCCCTC GTCAGCCTCC TTCTCCTCTC 60
ACCTCCAGGG TTCACGCATC TTGGATCATG AATGAGACAC TGAATGTGAT AGGCCCAGCA 120
GAGTGCTTAG GGTGCAGGGG TTCCCAATCC CCCATCGGCT CCAGCCGGCC GTCCTTAAGT 180
GTGGACTGCC AACAGCCGAT GCCCGGCCTA GAGGACATGC GGAGGCAGCA CAGTGTGAGA 240
GAGAAAAATC ACGCAAGCCA CAAAAGCACC TGACCGCAGG GCCACTGCAA GCCCCCATGG 300
AGGCTTTGAA CAATCAGAAA AGGTGCTCCT TTCAGCAGGT GGCTTGGGAA CAGGTAACAC 360
CCTTGTGTGA ATTAGAGCAA GGCTCCACTT CCTCTGAGCC GCTGCAGAAC CAGGTACTGG 420
AGTCTGGCAA GCTGAGGGCC AGATGCATTT CAGTGCCCAC TTGGCCACCT GTCAAGTGCC 480
TTCAGGAGGG GCACAGCCTG TGGACTGTCC CTGGTGGCCT TGCCTGCCTG CCAGCCCATA 540
ACGTCATCCC TGCAGGAGGA GAGGCGCCAC CTTACTAAGG AGGTGGGGAT CTCAGACCCG 600
TGGGTGGGTC CTGAGCCATT CCACTTAGGG GCCGCTGGGG TCCGTGTTAC CAGGACGGCA 660
GGGGGGGCTA GACGCCCTGA CTGAAAGCAA TGCATCGGGC CCACCTGGAG GGGGCCAGCC 720
GGGCCTGGGC TGCAGAGAGC CTCCCAGGCA GCTCAGTGTC CTGGGTCTCT CCTCGAAGTG 780
TACAGGCTGC CTGACCCAGT CCTAGATTAT ATCCTCCTCT GTGTAAACTT GCCTCAAGCA 840
GCATGCCAGA CACCAACCAG TCTGGGCCCC TCCCTGGGGA AATCACACTA CTTCCCGCAT 900
GCTCTTTCTG GGCCTGAACC CAGAGCCCAG AGCCCTGGTC CCAGCCCAAA GTGCACCCCT 960
TCTGCCCTCC 970
|
