| Tag | Content |
|---|
EnhancerAtlas ID | HS184-13691 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:45951960-45953390 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr17:45952896-45952909 | TCCATTTGCATAT | + | 6.23 | | ZNF263 | MA0528.1 | chr17:45952490-45952511 | TCCTCCTCTTCTCCCAGCTTC | - | 6.37 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 45952450 | 45953070 | | chr17 | 45952355 | 45952602 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I047875 | chr17 | 45952477 | 45953430 |
|
Enhancer Sequence | ACCTCTGGTT GCTGCTGATG TTGGGGTTCT CTCCATCTAG GAAGGGCTCA CTGGTCCTGT 60
ACGTTTGCCC TTGCTGATAT GGGCTGGGAG AGCTCCTAAG TAATTTGGAG AGTGCATGTG 120
GGATCCTCAT TGTGCCCCCA CCTGCACCCA GGATGGAGAC AGAGACTATC TCTTACGTTA 180
GACTGGGGGC TTCGCAAGAA CACAGGCTGC ATCTTTTCCA GTATATTGTA GCTCTCTGAG 240
GCCAGAGAGC CCCCATTAGG GTGGGACTGT GTGTCTACCA TTAATACTTT TCCCTAAAGT 300
TGAGGACTCT GCCCCCTCCA CCTGCCCAAA CCTGTGGTCA GCAGGAGCCA TTCCACAGGG 360
GAGAGGGGCC TAGACAGCTG CCTCTCCCAA GTCTTCACTG ACTGCTTTCT CAGCTCCCCC 420
TCAGCCCCCT TTTCCGGGCC CCTGCCACCA CCAGGGGGGC AGCTTTGTCA TTTCCCCTCT 480
CCCACCCGGC TTCTTCTCTT CTCAGAAACT CTGGCCTGGC ATCTGCCTCC TCCTCCTCTT 540
CTCCCAGCTT CTTACCACCC TCATCCCTCT CCAGGGCCTC AGGGCAAGTA TTTGCCATCT 600
GCCATCTCCT TGCATTCCTG GGGCTGGCTC CCAGGCTCCC TGCTTCCCCG GGGGGGCCTG 660
AGAACCCTGC TCATCTGCCC TATACCATCA GAGCTGCCCT TGCCACCCTC AGAATGCCTG 720
AGTCCTTTGT TCCGCAGTCC CCCCCAAGGC CTCCTGGGGC TTGCAGTGCC AGGGCTGTTA 780
ACATCGTAGG CTGCCCTCAC CCCTCTGAGC CAGAGAGGCT ATCAAAGCAA GCCTGGGGGG 840
CCCCCTCTAG CGCCAGCAAC TCCCGGTGCC TCCCTCCTCC AGGTCTCCAT CTTCACCTCA 900
GGGAGACTCC CTGCCCTGAG AACCCACCAC TTCATATCCA TTTGCATATA CTTGTTGGTC 960
CAGCCCAAGC AAATTAATGC AAATGCAATC CAAACCAGAG GCAATGAAGC AGCAACGCTG 1020
GATGGCCCTG ATGCCAGGAG AGGAATCAAC GTCTGGAAGA ACCTCTTTTT CCTGAGATGG 1080
ACATTCAGGG AAACCGAGGG TGGAGAGAAG TGCATTCCTT GCTTGTGCAT TCCTGGCTGG 1140
GATGCCTGAT TCTCTGAAAA CTTTCCAGGG CCACTGACCT GAGTTGTGTA ACAGTGCTCT 1200
CCTTTTGCCC TTAGACCTCC TTTAACTGTG GCTCTTCTTT CACACACTTT CGATCTTTTT 1260
CCTTCTCTCT GATCTTCCCC TTCCCTGGGT CCTGACACTC CTTGCCCTCA GCACAGGAGC 1320
CCTGCACCCC ACCATCATTC CCTGAGGGTG AGTGAAGCAG GTGGTTCCTG TGGACTCTGA 1380
GAAGAACTGA GGAGCCTCCC CTGTCACAGT GAGCTCCCCA CTAACCTGCC 1430
|
