| Tag | Content |
|---|
EnhancerAtlas ID | HS105-36262 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr17:79450870-79452190 |
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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I081482 | chr17 | 79449293 | 79452220 |
|
Enhancer Sequence | ACAGGGGCTG GTTTGGCCGA GGGACCTGCT TCTTGGGCAG CACCAGGAAA CAGCCGGAGA 60
CCCTCCCAGC GCCCACATCC ATGGCGTGAG CCCCGCGTGG GTGCAGCCCC TTCCGCAGCC 120
CGAATTCCAG GCCAGCCGCT GCAGGAGGGA CCGCCAGCCA GGGGCGCAGG GCAGAGGGTG 180
GGGGAAGGCG TGGCGCTCGC GCTCTCGGCT CTTGCTTGGA TGGCGCCGGC TGAGGACCCC 240
CACACCTGCG CTGCGGTGCA GAGGTCTTAG GATCCGAGGG GGCTGCCGGT CTGGGCCGGC 300
GCGTTCAGGC CCCGGGCGGT GGGGCGGCCT CGGCGTGCGT GGCTCGGTTG CCTGCAGGCA 360
GGCACGCGGC GCTGTGAGAA ACGAACGTCC GTGACTTAGC CCACGGGACC GTTTCTGCAT 420
TTTCACCCCA ACCTGGAGAG CTGCAGCACA GCCGCGGGAC AGGAAGTCGC CGCCAGGTGG 480
GTCAGGACTG CGACCTGAAC TCGGCTCTGC GGCCTCCCGC TCCGGCCGCC GGTTCGCAAT 540
CCTGGCGTGA ACCAGCAGAT CAACCTCCGG CGCCCGCCAC AGGCGCCCTC CCGCGGGAAC 600
CGGCAGGCAG GAGCGGTGCG GGGGCGCCCT CCAGCGGCCG TGGCCGGGAT GGCGGCCTCC 660
TGCCAGGCTC CAAGCGTGGC CGCGTGGGCA GCGCGCGCAG CCCGCCACGG AAAGACAGGC 720
GCTCCTCCTG GGTGGGCCTT GGGACCCCTT CGCGCCCTGT GTGGCCGCCT CGTGGTGAGC 780
ACCCCCGCCC CTCCCTGCAA GGCCGGTGTT CCCAGCTGGA AGGGCAGGCA ACCTGGGAAC 840
CAGAGGGAGC TGCTCTGGTT GGGAGGAAAA AGCCAGCTCG GTTCCCGCCT GAGCCCCGAA 900
GGGGCGGGGC TGGGAAGGGG GCCTGGCCAG AGGGAAGGAG CACTCTGGGT TGGGGGTGCT 960
GGGGGAGCAC AAAGGCAGGA ACTGGGGAGC ATAAGGCCAG GAGATAGGGG AGAACCTAGG 1020
CAGGAGCTGG GGGAGCAGCC AGGCAGGAAC TGGGGAGCAT CGATGCAGGA GCTGTGTCGC 1080
GTGTTATCCC CGTCACGTGG AGTTGTGTGT CCTGCGAGGA GCACAGCATT TCAGGGCCTA 1140
GAGCCCCTCT CTGTACTGGA GCCGCCTGTG TGTGTCCATT CCGAATGAGC CATACTTCCC 1200
TCGCAGCTCT CCCAGTGGGA TTGAGAACTG TTAGGCACAC ACCTGGTGAA GCATTGCTGC 1260
CCTTTCTGTT GGGGAGAAGC GGCCTTCTAG CGCAGAGAAT AGCTGCTTCC TGGAACTGAA 1320
|
