| Tag | Content |
|---|
EnhancerAtlas ID | HS076-56569 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr9:119333590-119334850 |
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 | chr9:119334618-119334637 | GAGCGCCCTCTGTTGGCTG | - | 6.48 | | SPIC | MA0687.1 | chr9:119334664-119334678 | GACTTCCTCTTTCC | - | 6.14 | | Sox3 | MA0514.1 | chr9:119334209-119334219 | CCTTTGTTTT | + | 6.02 | | ZNF263 | MA0528.1 | chr9:119334467-119334488 | TCTCTCCCTGCCTTCTCCTCC | - | 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 |
| GH09I116572 | chr9 | 119334280 | 119335170 |
|
Enhancer Sequence | CCAAGCTGAG CACTCAATCT GGACTCCAGC CCTCCTTCCC TGGGTCTTCT CACTTTTCTT 60
CTATTCTGTC TCTTTTTCCA TCTTTCACAA CCCTTTCTCT TTCCCTATTT CTGGCCTCTC 120
CCTCTTTTCT CTTTTAGAAA CATTTACTGA ATTACAAGTG CTTTTGATCC ATGTGGAGTT 180
ATGTCCATAC GGTGAGTGTG AGTATTTGGT GTGTGCTGTG CTGTGGGTGC TACGTGAGTG 240
GATGCCATCT AATGTGTCTG TGTCTGTTTG TGCTGGGTGG ATCCATGTGG CACACGGTAT 300
GTATATCTTT ACAGTATGCC TGTGGGAAGG TGGCTATGTT TACGCATCTG TGTGCCTGTG 360
CTGTTTATCT ATGATACGCC TCTTGAGGCA TCTGTCATGT GTTGAGTACA AGCTGTGTGT 420
TGTCTGTGCG TGGCATGCTA TCCCCATGGT GTGTAACTTT GTATGTGTTG TGGATCTACT 480
GTATGTGTCT GTGTGCTTCC CGTGTGTGTG TGACCGTGTC TCTTTGTTAT CTGCCTTTCG 540
TTGGCTGCAC ATAGCTTGAA TGTCCCTGTT GGGTGATGTG CTCACATGCA TGTTTATATG 600
TGTTGGTATC TGTGTGTTGC CTTTGTTTTT GTTTAGCTGG CTGAGGTGAC TGCATTGTGT 660
ATACCTGTAT GGGATGGATT GCATTCATTT GTGAGTCTGC ACCCTATATG ATTTCTCTAA 720
ATCCCCTGGC TGCATGCTGT GTCTGTGTGG GGTATGTTGC ATTTGTTGTT TGTAGGTACA 780
ACTGCATATT CTGTGTGTTC CCCTGTGTCT CTGCCTCTGT GAAATGTGTC TGTGTGTTTT 840
CCCTGCCAGC TCCTCCTCCC CTTCGGGTGC CCCAGCCTCT CTCCCTGCCT TCTCCTCCCC 900
AGGCTGTGAC CACTCTCAGC TGACACCTCC GCTGCTCTGG CAACCCAAGA ACAGCCTGGA 960
GAAAGGTCAG CTGGCCGCCT TCCCCAGGGC CTGCCTGGAT CCTTGGACCC CAGTGTTGCG 1020
TGGTGTGGGA GCGCCCTCTG TTGGCTGTAT GGGCCATGAA CACCACTGGA AACAGACTTC 1080
CTCTTTCCCT TGCTGCTCAC CCCTGAGACT TCCAGCCTTC TTAATAAGGG ACTTTAGGAG 1140
AGGAATGGGT AGGGTCGCCT ATAATTTGCC GTTGAAAGCG AGATGTTTTG GAGAATGAAA 1200
GAGGGTGTGA ATAAGTGCAC TGAGATACTG AGTATTCGGC AGATGCGTCT TAAGCAGATG 1260
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