| Tag | Content |
|---|
EnhancerAtlas ID | HS023-25504 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr9:107730060-107731670 |
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 | GAGTTCAAGA CCAGCCTTGC TGACATGGTG AAACCCAGTC TCTACTAAAA ATACAAAAAT 60
TAGCTGGGTG GTAGTGGCAC GCGCCTGTAA TACCAGCTAC TTGGGAGGCT GAAGCAGGAG 120
ACTCTCTTGA GCCTGGGAGG CAGAGGTTGC GGTGAGCCGA GATCGCGCCA CTGCACTCCA 180
GCCTGGGCAA CAGGGTGAGA CTACGTCTCA AAAAAAAAAA AAAAAAAAAA AAAAAAGAAG 240
AAGAAATTTA ACATACAGGC GATTTTTCAG GTTCTCATTT GCTAAACCAA CAATGCAGAA 300
TTTGTGAAGT AGGGGCAACA AGTTGCTGAA CCTGAGAGAC GCCTCTAAAT GCGCTCAGAG 360
GTTATTTCAA CTGTGCTGTT TGCTAGTTCA GGTACAACAG GCAAGACAGA AAGATGCCAC 420
CGCTCTCTCC ACCCTCCCAG CGCCGGATCA CAGAGCGCAG ACCATGCACC CAGCCTTCCA 480
CACACGTCGC GATCTCGCCG CTTTAAGCTG CTGGGTACCC TCGGCCCGCC CACAAGAAGG 540
CGGGGCGGCG CGGGGTCTGC TGGGAGTTGT AGTTTCGGGC CGGGCCCGAG AGCTTCTTGA 600
CTCGTTTCCT TCTACCCCCA CCGCCGCACA GCTGCCTATG GACTCTGGAG TTGCTGTGTA 660
TTGAGCATGG GGCACAGCCG GGGGTAAAAG GGGAGAAGGC TCCTTTAATC TGCGGATCGG 720
GGCGCCGTTG ATGAGTGTTA GAGGTGTTGG AACGCAGAGT AAGCGGCGCG CATGCGCGGC 780
TGCCGGAGGT GGGGGCCGCT CCTCCCGTGC CACTCAGGGG CTGGCTGCTG CCTTAGGGCT 840
GACTGGGCTC ATAGGTAGGG CCTGCGGTGC AAGTTTGTGA TAACACTGCC TGTAGGCTGC 900
GGTTGTTAAG GCAGAGATTT GAAGGGGGTC GGTTGGGGGT GCTGGGTAGT GTCAGTAATC 960
AAGGGTTTTA ATCGCTACTC CATCCTGGCT TTCGGGAACC TCCCACCTCC TACCCTTTCC 1020
CAGTTTGCAG AATTGCAGCT TTCCCCATCC CCCACCCCGA TCGCTTCGTG GGAAGCCTTT 1080
CCATACTGTG TTGTGAAATC CGTTAGACCT CAGCCAAGGC CTTTTAGCCC GCCCGGAATT 1140
CAAGCTGCCC CCTCCTTGCC AAATCCAGAT CATGCGAGAC AACAAAAGGC TTGAGGCACA 1200
AGCCCTACAA GGCAGTGCCC CTGCCAGTTC TCCTAAACTT ATTGTTTACC CTGCCCTCTT 1260
CTTCCCCTGC AAATTCAGAC AGCCAGGCGA TAGATTAGAT AAATAGATTC CATGTCCTTA 1320
CATTTGCAAC AGGCTTTCAT AGATTCCTTT GCTCTGGAAG GTGGCATCAT TATACAAAAG 1380
GACAAGTGAG AACACACGAA TGTAATCAGT GGCAGAACCC TGGGACTGAA CCCTACAGGA 1440
GTTCTAAGTC TATTGTTTCT CCTACCACTT CACAAATGTG TCAGAAAGAG CTGAATGAGG 1500
TGACCAGCTG CACCTGACGC TAGCTGGCTT TCGGAATGCT CAGGCCCTGG GCCCTTGGCT 1560
CACCACAACC ACTCTTAAAT TGACTAACAA TTGCCCCTTA GTGAGTGACC 1610
|
