| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08351 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:102288160-102289040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr12:102288700-102288711 | GATGAGTCACC | - | 6.32 | | JUND | MA0491.1 | chr12:102288700-102288711 | GATGAGTCACC | - | 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 |
| GH12I101894 | chr12 | 102288127 | 102289389 |
|
Enhancer Sequence | CTGGGATTAC AGGCATGAGC TACCACACCC GGCCAATTTT TGTATTTTTT GTAGAGACAG 60
GGTTTCACCA TGTTGCCCAG ACTGGTTTCG AACTCCTGAG CTCAAGTGAT CCATCCTCCT 120
CGGCCTCCCA AAATGCTGGG ATTACAGGTG TGAGCTACCG TGCCTGGCCT CCACCTGTAT 180
GGTTTTAAAT GTACAGATAA GCAAGAATAG AACACGACCC TGGAATTCCA AGTTTTCAGA 240
TCACGTGTTT GATGTCATGT GGACTCCACA CCTGGGCCTT TGACATAGTC TCAATTTGCC 300
ATCAATAGAC AGAGTCCCCA GGTCTGGTCT TCTCTTCAGT CAGAGCACCT AGAGCACCTT 360
CATATCGCCA CCTCCCTATC TTCCTAAATA TCCTCCTCAT TCTTTCATTG CCTTCCCTTT 420
CTCCACAGAC AGGCAAACAA CCTTCTTCCC AGCGCTTCTC CTCTGTGTTT GCTCCGATGC 480
CTGGCATGTG GCTGTCTGAG GTTCAGAATT ATTCTCAGAC CTGTGTAACA AGAACTCTAG 540
GATGAGTCAC CTGGTGCCTG CTTTTTTATA CCCTCAGGCC AAGGCAGGGA GGCCTGATTT 600
CCCTGGCAGA GTTAATTGTG TGGCAAAAGT GCTGCCCAAG GTTATGAGCT GTCTCTGCTT 660
TTTTCCCCAT TACTGGTTCC CATTCCTGTC TCTCTGCCCA TTCAGCATTG TGCTCAGAAG 720
GGCATCCTCC ACCTCAACAT TCCTGTAGTG TGAAAAATGG TTATTGTAGG AAAAGTGGTA 780
ATGCTAAATT CGAAACCCTT CAGGTTTTTT TTTTTTTTTT TTTTTTTTTT TTTTACCCAG 840
GCTGGAGTGC AGTGGCGTGA TCTCAGCTCA CTGCAAACTC 880
|
