| Tag | Content |
|---|
EnhancerAtlas ID | HS098-58692 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:128136590-128137590 |
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 | chr9:128137171-128137190 | GGGTGACATCTTGTGGCCA | - | 6.09 |
|
| | 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 |
| GH09I125374 | chr9 | 128136680 | 128137462 |
|
Enhancer Sequence | CCCTTCAGGG CGGGGATTCC ACCATCTTTT CCTTCCAAAT TCAGGCCCTG CTGGGACAGG 60
AACTATCCCT GTCGTGGTCC AGGGCCAGGT AGTTCTTCAC GTCCTCTGGG AAGACAGAGT 120
GCCCCAAAGC CCTTGATCTC CAGTGGGTAG AATTAGGTGG GGCAGAGGCT GTGCCACACC 180
AGGTCACACC TCTCCTGTGT CTGCTCCCAC CCCACCAAGC ACAGGGCCGG GATGAGGATG 240
CCTGGAGCCC AGCTCAGTGC CTGCCTGGGT TGCAGCCCTG ATCACACCAA AGTGTCTTGT 300
CTGTTTGCAG CCCTTTATCT GGCTAGCAGG GTTTAATTTT ACTCTGGGAA GGTGGGATTT 360
TTGTCCCTAT TTACTTATTA TTTTCGAATT TATTATCTTT AGGTGGCATC TACAAATCGG 420
CGTCCTCTGA GGGCAACAGC GCCCCGTTCT GCTAGAAATC CCGAGATTTG CAGCCACTGC 480
AGCACGCTGC CTCTGCGGCT TCTCCGCACC ATCCCCGACC CCTTCCCCCG CGAGTCTGCC 540
GTCGGCCAGT TTCCTCCCAG GCCCCGGCTT TGCTGTTCCT TGGGTGACAT CTTGTGGCCA 600
AGGACAGGTA CAAACCATTG GCTGAAAAGG AGGAGCAAAG GCAGCCCTCA GCCCTCTCTG 660
GAGGAGCCTT GGGGCGCCTT CGAGGATGCC CAGGAGGGCA GGGGGCTCCT GAACAGGGAA 720
TCGGCTCTCA GACCCCGAAT GGGCTTGCAC CAAGCCCTTC ATGAGACAGC TGTGGCTGGA 780
GCCCAGAATT CACCCAGGCC CCCCGAGGCA GACACACCAG GTTCCTCTCT GCCCACCCTG 840
CGTTGTGGCA AATAATCATT ATTCCCGATA TAAAGCTTTT CTCTAGCAGC CCAACGACAA 900
GGTTATTATT CCAATCTTAC AGATGCAGCA ACAGCCCTGA GCCACAGCCA GTGACCTGAG 960
CCCAGCCCAC AGGTGCCAAC ACTGTAAGAT CTCACTGGAC 1000
|
