| Tag | Content |
|---|
EnhancerAtlas ID | HS184-30211 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr8:120779660-120780510 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr8:120780170-120780189 | CACTGCCACCTCGAGGCCA | - | 6.19 | | TFAP2A | MA0003.3 | chr8:120780480-120780491 | TGCCTGAGGCT | - | 6.32 |
|
| | 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 |
| GH08I119767 | chr8 | 120780021 | 120780230 |
|
Enhancer Sequence | GGGGAAAGGA TAAGTGAGTG AGAGATCCCT GGGGTTCCAC ACTCCTACTA AGAACTTTTA 60
CAATCCTAGC AGCAGGGAGC CGACACCTCT TGGCCCCTCA GGCTTCCAGT CTAATACAGT 120
GAGCTGCCCG AAGACTGTAG AGACGCTGCT GGAGTCTACG TGGAATCCCA CAGGCTTTGG 180
CCCCTGAGCA GTCAGGTGCC AGCTGCTACT GCCCCACCAG GGAAGGAGCA GGCAGACCCG 240
GCATTTTCAC ACAACCCAAA GACAGATACG GCAGCCACAG TACAGAGCAG CAGGCAGACA 300
GCAGAATGTG AAGAAAGTCT GCTTCAGCTA CTGTTTGCTG AACAGGTCCC TGCTTCTTCA 360
GCGCTGGGTC CACAGTGCAG CCGCCCTGCC ACTGCATGTG TATTTTGGCT GTGGCCCAGT 420
GTAGTGAGAG CCCAGCCCCA AGAAGCCAGG GACCTGCCCT TTGGCTCCTG CCACAGCAGT 480
TTTTGTCACC ACAGGCCACC ACAGATGCCA CACTGCCACC TCGAGGCCAG GGAGAGAGGG 540
GGAGGCTGAG CACGTTTGCA TGTCCCCAAC AGCGAAATAC ACCTCCACTC CTATAAAAGG 600
GAAGTGCAAT CGGGCCACGC ATCCCACAGC TGCCAGCCTC CCTTGCTCCA GCTGAGGGAG 660
TCCGCCTTCC TCAGCGAAAG AACAGCAGCA CGGCCACCCT GCTCCCACCC AACCGTTTCA 720
GCTGCCAGCT GGAGCCCTTC TGAGAGCCCA TGCTGACAGG TCTGTGATCA ACCCTGGGGT 780
TCCCACCACC TGCGTATTCT GCCACCAACT CAGCTGTTAC TGCCTGAGGC TTCCCATACA 840
CCATCGAGCA 850
|
