| Tag | Content |
|---|
EnhancerAtlas ID | HS077-11489 |
Organism | Homo sapiens |
Tissue/cell | H128 |
Coordinate | chr9:107730260-107731400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr9:107730827-107730838 | GCGCATGCGCG | + | 6.02 | | NRF1 | MA0506.1 | chr9:107730826-107730837 | CGCGCATGCGC | - | 6.02 |
|
| | 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 |
| GH09I104967 | chr9 | 107730021 | 107731977 |
|
Enhancer Sequence | CTACGTCTCA AAAAAAAAAA AAAAAAAAAA AAAAAAGAAG AAGAAATTTA ACATACAGGC 60
GATTTTTCAG GTTCTCATTT GCTAAACCAA CAATGCAGAA TTTGTGAAGT AGGGGCAACA 120
AGTTGCTGAA CCTGAGAGAC GCCTCTAAAT GCGCTCAGAG GTTATTTCAA CTGTGCTGTT 180
TGCTAGTTCA GGTACAACAG GCAAGACAGA AAGATGCCAC CGCTCTCTCC ACCCTCCCAG 240
CGCCGGATCA CAGAGCGCAG ACCATGCACC CAGCCTTCCA CACACGTCGC GATCTCGCCG 300
CTTTAAGCTG CTGGGTACCC TCGGCCCGCC CACAAGAAGG CGGGGCGGCG CGGGGTCTGC 360
TGGGAGTTGT AGTTTCGGGC CGGGCCCGAG AGCTTCTTGA CTCGTTTCCT TCTACCCCCA 420
CCGCCGCACA GCTGCCTATG GACTCTGGAG TTGCTGTGTA TTGAGCATGG GGCACAGCCG 480
GGGGTAAAAG GGGAGAAGGC TCCTTTAATC TGCGGATCGG GGCGCCGTTG ATGAGTGTTA 540
GAGGTGTTGG AACGCAGAGT AAGCGGCGCG CATGCGCGGC TGCCGGAGGT GGGGGCCGCT 600
CCTCCCGTGC CACTCAGGGG CTGGCTGCTG CCTTAGGGCT GACTGGGCTC ATAGGTAGGG 660
CCTGCGGTGC AAGTTTGTGA TAACACTGCC TGTAGGCTGC GGTTGTTAAG GCAGAGATTT 720
GAAGGGGGTC GGTTGGGGGT GCTGGGTAGT GTCAGTAATC AAGGGTTTTA ATCGCTACTC 780
CATCCTGGCT TTCGGGAACC TCCCACCTCC TACCCTTTCC CAGTTTGCAG AATTGCAGCT 840
TTCCCCATCC CCCACCCCGA TCGCTTCGTG GGAAGCCTTT CCATACTGTG TTGTGAAATC 900
CGTTAGACCT CAGCCAAGGC CTTTTAGCCC GCCCGGAATT CAAGCTGCCC CCTCCTTGCC 960
AAATCCAGAT CATGCGAGAC AACAAAAGGC TTGAGGCACA AGCCCTACAA GGCAGTGCCC 1020
CTGCCAGTTC TCCTAAACTT ATTGTTTACC CTGCCCTCTT CTTCCCCTGC AAATTCAGAC 1080
AGCCAGGCGA TAGATTAGAT AAATAGATTC CATGTCCTTA CATTTGCAAC AGGCTTTCAT 1140
|
