| Tag | Content |
|---|
EnhancerAtlas ID | HS184-14400 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:79451010-79452220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr17:79451770-79451780 | GGGGCGGGGC | - | 6.02 | | SP2 | MA0516.2 | chr17:79451767-79451784 | GAAGGGGCGGGGCTGGG | - | 6.21 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_61461 | chr17:79399734-79459539 | Toledo | | SE_68550 | chr17:79437775-79457671 | TC71 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 79451287 | 79451558 | | chr17 | 79451546 | 79452200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I081482 | chr17 | 79449293 | 79452220 |
|
Enhancer Sequence | GCAGGAGGGA CCGCCAGCCA GGGGCGCAGG GCAGAGGGTG GGGGAAGGCG TGGCGCTCGC 60
GCTCTCGGCT CTTGCTTGGA TGGCGCCGGC TGAGGACCCC CACACCTGCG CTGCGGTGCA 120
GAGGTCTTAG GATCCGAGGG GGCTGCCGGT CTGGGCCGGC GCGTTCAGGC CCCGGGCGGT 180
GGGGCGGCCT CGGCGTGCGT GGCTCGGTTG CCTGCAGGCA GGCACGCGGC GCTGTGAGAA 240
ACGAACGTCC GTGACTTAGC CCACGGGACC GTTTCTGCAT TTTCACCCCA ACCTGGAGAG 300
CTGCAGCACA GCCGCGGGAC AGGAAGTCGC CGCCAGGTGG GTCAGGACTG CGACCTGAAC 360
TCGGCTCTGC GGCCTCCCGC TCCGGCCGCC GGTTCGCAAT CCTGGCGTGA ACCAGCAGAT 420
CAACCTCCGG CGCCCGCCAC AGGCGCCCTC CCGCGGGAAC CGGCAGGCAG GAGCGGTGCG 480
GGGGCGCCCT CCAGCGGCCG TGGCCGGGAT GGCGGCCTCC TGCCAGGCTC CAAGCGTGGC 540
CGCGTGGGCA GCGCGCGCAG CCCGCCACGG AAAGACAGGC GCTCCTCCTG GGTGGGCCTT 600
GGGACCCCTT CGCGCCCTGT GTGGCCGCCT CGTGGTGAGC ACCCCCGCCC CTCCCTGCAA 660
GGCCGGTGTT CCCAGCTGGA AGGGCAGGCA ACCTGGGAAC CAGAGGGAGC TGCTCTGGTT 720
GGGAGGAAAA AGCCAGCTCG GTTCCCGCCT GAGCCCCGAA GGGGCGGGGC TGGGAAGGGG 780
GCCTGGCCAG AGGGAAGGAG CACTCTGGGT TGGGGGTGCT GGGGGAGCAC AAAGGCAGGA 840
ACTGGGGAGC ATAAGGCCAG GAGATAGGGG AGAACCTAGG CAGGAGCTGG GGGAGCAGCC 900
AGGCAGGAAC TGGGGAGCAT CGATGCAGGA GCTGTGTCGC GTGTTATCCC CGTCACGTGG 960
AGTTGTGTGT CCTGCGAGGA GCACAGCATT TCAGGGCCTA GAGCCCCTCT CTGTACTGGA 1020
GCCGCCTGTG TGTGTCCATT CCGAATGAGC CATACTTCCC TCGCAGCTCT CCCAGTGGGA 1080
TTGAGAACTG TTAGGCACAC ACCTGGTGAA GCATTGCTGC CCTTTCTGTT GGGGAGAAGC 1140
GGCCTTCTAG CGCAGAGAAT AGCTGCTTCC TGGAACTGAA ATCCTGCCGC ATCCAGACCA 1200
AGAGCATGCT 1210
|
