| Tag | Content |
|---|
EnhancerAtlas ID | HS184-12462 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr16:57443830-57444920 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr16:57443961-57443980 | AGCTGCCCCCTCCTGGTCA | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr16 | 57443864 | 57444508 | | chr16 | 57444556 | 57444606 | | chr16 | 57444650 | 57444806 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I057409 | chr16 | 57443197 | 57444603 |
|
Enhancer Sequence | TCAGCTGTCA GCGATGGAGA TGAGTAAACA AATGCTCAAT CCTTACTGAG CTGCTCCGGG 60
AGACCTCGGG CAAGTCACTG CCCTGATGAG CCTCAGGTGA CACTGGTGTG ACCGGGATGA 120
CACTTCTGCC TAGCTGCCCC CTCCTGGTCA GCCACAGCTG TCAAATGCAA CTGAAGATGA 180
TGAAGAGCTG CCGCCCCAGC CGCTTGGCTG CCCTGTGACT GAGAGCATCC TGGTTCCGCC 240
CACTGCCTCG GGGACAGGCT TCTCCACGAG CCTGGGCAGA GCCTGGGGTT GGGGCAGGAA 300
CCTTCCTTCC CTGTCTTTCA GGGAGAAGGA CCCCATATCT GCCTGGCCCA GTGCCCTCTG 360
GCTAAAGCCG AGTTGGGTGT TGCAGCAGCC CCTGGGGCAA GGGCGGCAGG TGCCTGGGTG 420
GTGTGCCTGG CCACTTTAGT CAGAGGCGTT GAGACAAGGA GTTACCACAG CCGCTCCTCC 480
CACTCAGATC CAATTACCCT TCACACTCTC CTAATAGGCC TAACAGTGTC TGGCCTGCTT 540
CCCTGCCATG GCCCTTTCCC TTCCTTTGGC CACAGCACTC TCTCCCCTGC TGCCCCTCCA 600
CAAAGCTCTG CCTCACTGCC ACTTCCTCCA GGGAGCATTC CTGATTGCCC TGACAGACCT 660
CCAGGTCCTA GAATCCTCAC AGCAGCATAA AGATCTCTCA AGATGCTTCT CACAGGCCCA 720
GACTTCAGAA TAGTTTGTCT GGAAGTTCCC TTGGCATCCA TCCCATAGCC TGGGAGAACT 780
GAGGAGGGAT AAACTCGGTT AATCCCTGGA GAGGAAACCA CCTCAAAAAT GTCCCTGGTC 840
CCCGCTGCCT CCCAAAGAAG ACTGAGGCAC ACTGGGCCCT TTGCATCCAT CTCGCCTTCC 900
CTTCCTTCAG TCCTGTGTTT ACTCGGTCAG GTGACACTGA AGGTTCACTG CATGCCAGGC 960
ACCATGCTTG GTGCTGGGGA TGCCCACGGC GCGGGGCAAG GTAGACACAG CCAGTCCTCG 1020
TGTGACTGGC TCTTAGCCTT GCATTTAGGC AGTGCCCCAT GCCGGGGTTT CATGCTGTTG 1080
CCCTAATTTA 1090
|
