| Tag | Content |
|---|
EnhancerAtlas ID | HS007-17448 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr9:107730320-107731400 |
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 | GATTTTTCAG GTTCTCATTT GCTAAACCAA CAATGCAGAA TTTGTGAAGT AGGGGCAACA 60
AGTTGCTGAA CCTGAGAGAC GCCTCTAAAT GCGCTCAGAG GTTATTTCAA CTGTGCTGTT 120
TGCTAGTTCA GGTACAACAG GCAAGACAGA AAGATGCCAC CGCTCTCTCC ACCCTCCCAG 180
CGCCGGATCA CAGAGCGCAG ACCATGCACC CAGCCTTCCA CACACGTCGC GATCTCGCCG 240
CTTTAAGCTG CTGGGTACCC TCGGCCCGCC CACAAGAAGG CGGGGCGGCG CGGGGTCTGC 300
TGGGAGTTGT AGTTTCGGGC CGGGCCCGAG AGCTTCTTGA CTCGTTTCCT TCTACCCCCA 360
CCGCCGCACA GCTGCCTATG GACTCTGGAG TTGCTGTGTA TTGAGCATGG GGCACAGCCG 420
GGGGTAAAAG GGGAGAAGGC TCCTTTAATC TGCGGATCGG GGCGCCGTTG ATGAGTGTTA 480
GAGGTGTTGG AACGCAGAGT AAGCGGCGCG CATGCGCGGC TGCCGGAGGT GGGGGCCGCT 540
CCTCCCGTGC CACTCAGGGG CTGGCTGCTG CCTTAGGGCT GACTGGGCTC ATAGGTAGGG 600
CCTGCGGTGC AAGTTTGTGA TAACACTGCC TGTAGGCTGC GGTTGTTAAG GCAGAGATTT 660
GAAGGGGGTC GGTTGGGGGT GCTGGGTAGT GTCAGTAATC AAGGGTTTTA ATCGCTACTC 720
CATCCTGGCT TTCGGGAACC TCCCACCTCC TACCCTTTCC CAGTTTGCAG AATTGCAGCT 780
TTCCCCATCC CCCACCCCGA TCGCTTCGTG GGAAGCCTTT CCATACTGTG TTGTGAAATC 840
CGTTAGACCT CAGCCAAGGC CTTTTAGCCC GCCCGGAATT CAAGCTGCCC CCTCCTTGCC 900
AAATCCAGAT CATGCGAGAC AACAAAAGGC TTGAGGCACA AGCCCTACAA GGCAGTGCCC 960
CTGCCAGTTC TCCTAAACTT ATTGTTTACC CTGCCCTCTT CTTCCCCTGC AAATTCAGAC 1020
AGCCAGGCGA TAGATTAGAT AAATAGATTC CATGTCCTTA CATTTGCAAC AGGCTTTCAT 1080
|
