| Tag | Content |
|---|
EnhancerAtlas ID | HS187-25138 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr9:107730010-107731370 |
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 | | Nr2f6(var.2) | MA0728.1 | chr9:107730052-107730067 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | 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 | GTAATCCCTG CACTTTGGGA GCTCAAGGTG GGTGGATCAC CTGAGGTCAG GAGTTCAAGA 60
CCAGCCTTGC TGACATGGTG AAACCCAGTC TCTACTAAAA ATACAAAAAT TAGCTGGGTG 120
GTAGTGGCAC GCGCCTGTAA TACCAGCTAC TTGGGAGGCT GAAGCAGGAG ACTCTCTTGA 180
GCCTGGGAGG CAGAGGTTGC GGTGAGCCGA GATCGCGCCA CTGCACTCCA GCCTGGGCAA 240
CAGGGTGAGA CTACGTCTCA AAAAAAAAAA AAAAAAAAAA AAAAAAGAAG AAGAAATTTA 300
ACATACAGGC GATTTTTCAG GTTCTCATTT GCTAAACCAA CAATGCAGAA TTTGTGAAGT 360
AGGGGCAACA AGTTGCTGAA CCTGAGAGAC GCCTCTAAAT GCGCTCAGAG GTTATTTCAA 420
CTGTGCTGTT TGCTAGTTCA GGTACAACAG GCAAGACAGA AAGATGCCAC CGCTCTCTCC 480
ACCCTCCCAG CGCCGGATCA CAGAGCGCAG ACCATGCACC CAGCCTTCCA CACACGTCGC 540
GATCTCGCCG CTTTAAGCTG CTGGGTACCC TCGGCCCGCC CACAAGAAGG CGGGGCGGCG 600
CGGGGTCTGC TGGGAGTTGT AGTTTCGGGC CGGGCCCGAG AGCTTCTTGA CTCGTTTCCT 660
TCTACCCCCA CCGCCGCACA GCTGCCTATG GACTCTGGAG TTGCTGTGTA TTGAGCATGG 720
GGCACAGCCG GGGGTAAAAG GGGAGAAGGC TCCTTTAATC TGCGGATCGG GGCGCCGTTG 780
ATGAGTGTTA GAGGTGTTGG AACGCAGAGT AAGCGGCGCG CATGCGCGGC TGCCGGAGGT 840
GGGGGCCGCT CCTCCCGTGC CACTCAGGGG CTGGCTGCTG CCTTAGGGCT GACTGGGCTC 900
ATAGGTAGGG CCTGCGGTGC AAGTTTGTGA TAACACTGCC TGTAGGCTGC GGTTGTTAAG 960
GCAGAGATTT GAAGGGGGTC GGTTGGGGGT GCTGGGTAGT GTCAGTAATC AAGGGTTTTA 1020
ATCGCTACTC CATCCTGGCT TTCGGGAACC TCCCACCTCC TACCCTTTCC CAGTTTGCAG 1080
AATTGCAGCT TTCCCCATCC CCCACCCCGA TCGCTTCGTG GGAAGCCTTT CCATACTGTG 1140
TTGTGAAATC CGTTAGACCT CAGCCAAGGC CTTTTAGCCC GCCCGGAATT CAAGCTGCCC 1200
CCTCCTTGCC AAATCCAGAT CATGCGAGAC AACAAAAGGC TTGAGGCACA AGCCCTACAA 1260
GGCAGTGCCC CTGCCAGTTC TCCTAAACTT ATTGTTTACC CTGCCCTCTT CTTCCCCTGC 1320
AAATTCAGAC AGCCAGGCGA TAGATTAGAT AAATAGATTC 1360
|
