| Tag | Content |
|---|
EnhancerAtlas ID | HS184-22007 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr3:185976800-185977880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:185977490-185977509 | CGGCCAGTAGAGGGCTCTC | + | 6.25 | | Mafb | MA0117.2 | chr3:185977828-185977840 | AAACTGCTGACT | + | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH03I186260 | chr3 | 185976881 | 185977030 | | GH03I186259 | chr3 | 185977041 | 185978090 |
|
Enhancer Sequence | GGTGGTCTGA GAAGAGCCCT GGAGCTTTCA GAATCACTGA TGCATGTGTA GGCAAATTAA 60
CATTCCTTCT CTTGCAGAAC TCTGCTCTCC GACGGGACTC TCCGACGGGA AGTGAATTCT 120
GAACAGACGC TCCCTCCAGC TAGGCAGCTT GTCTGATTAG AGAGTGACAT GCGCATGAGA 180
GACCCTCAGG GCGTATCAGC CCGGGAAGTA GCCACCTGGC TCGTCGTCTC AGATGAAAAC 240
AATTTAGAAT ACACGAGGTG AAGCTGGAGG ACTGTCTGCC AGTTTTGACA GTGGGCTGGT 300
AAAGGTGTCT GTGGGGGGCT GCTCCGTCAC AAGGCTGTAC TGTTCAGCAG TGATGGCAAT 360
CACGGTGACT GTGATGGCAA CTGCAGTGGT GTACAGAGGT GGGCTCTGTT CTGAAATTAC 420
TTTTACAGGT AAATCATGGC AGGTGTACTG AATCCGCACT TATGTTTCTT TCTCTTTTTA 480
ACTGGGCCTT GTACTACCGC TGCCATAAAC AATAGCTTTG GTGTCAGCCA ACCAAAGACA 540
GGGTCAAATT CTCTTTTCAG AGTCCTTACT CCAACCTCTC TGAGGGGTCT AGCTGAACCC 600
GGAGCAGAAA TCCTGGTTTG GAGGTTGGGC AAATGGCTGC GTGCTGGGCA AGCCCAGCCC 660
AGAGTATGCA GACAGCCCCG GGCCCGGGGC CGGCCAGTAG AGGGCTCTCG AGCACCGGCC 720
CGGACTGGGA GGAAGCCCAG GCTTTCCTGG CCTTCTAGCC CAGGTGCTGT AGGGGCCGCA 780
TCACAGAGAC CTGCAGCTCA CCATTAGCCG CAGACACAGG GACCACGCCT CCCACCAGGC 840
CTCTTTACAA CCCCATGCTA ACGAGAAGAG AATAGCCAAT GAGTAAGTGG CAGGAGGAGC 900
AAAACAACCT CAAAATCGAA TGATTTAGAA AACAAAAGTG ATTCCATTGA ACAAGTAATT 960
GTCTTGATCC TAAAATGACC CCACAACGGA ACACCAAGGC AGAACTCTGA GTCACTGTCT 1020
AGATTTCCAA ACTGCTGACT GACAATGATA AGAAAACTTT CTCTTCTCTG ATGATTCAGT 1080
|
