| Tag | Content |
|---|
EnhancerAtlas ID | HS158-58319 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr9:107730370-107731700 |
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 | AGGGGCAACA AGTTGCTGAA CCTGAGAGAC GCCTCTAAAT GCGCTCAGAG GTTATTTCAA 60
CTGTGCTGTT TGCTAGTTCA GGTACAACAG GCAAGACAGA AAGATGCCAC CGCTCTCTCC 120
ACCCTCCCAG CGCCGGATCA CAGAGCGCAG ACCATGCACC CAGCCTTCCA CACACGTCGC 180
GATCTCGCCG CTTTAAGCTG CTGGGTACCC TCGGCCCGCC CACAAGAAGG CGGGGCGGCG 240
CGGGGTCTGC TGGGAGTTGT AGTTTCGGGC CGGGCCCGAG AGCTTCTTGA CTCGTTTCCT 300
TCTACCCCCA CCGCCGCACA GCTGCCTATG GACTCTGGAG TTGCTGTGTA TTGAGCATGG 360
GGCACAGCCG GGGGTAAAAG GGGAGAAGGC TCCTTTAATC TGCGGATCGG GGCGCCGTTG 420
ATGAGTGTTA GAGGTGTTGG AACGCAGAGT AAGCGGCGCG CATGCGCGGC TGCCGGAGGT 480
GGGGGCCGCT CCTCCCGTGC CACTCAGGGG CTGGCTGCTG CCTTAGGGCT GACTGGGCTC 540
ATAGGTAGGG CCTGCGGTGC AAGTTTGTGA TAACACTGCC TGTAGGCTGC GGTTGTTAAG 600
GCAGAGATTT GAAGGGGGTC GGTTGGGGGT GCTGGGTAGT GTCAGTAATC AAGGGTTTTA 660
ATCGCTACTC CATCCTGGCT TTCGGGAACC TCCCACCTCC TACCCTTTCC CAGTTTGCAG 720
AATTGCAGCT TTCCCCATCC CCCACCCCGA TCGCTTCGTG GGAAGCCTTT CCATACTGTG 780
TTGTGAAATC CGTTAGACCT CAGCCAAGGC CTTTTAGCCC GCCCGGAATT CAAGCTGCCC 840
CCTCCTTGCC AAATCCAGAT CATGCGAGAC AACAAAAGGC TTGAGGCACA AGCCCTACAA 900
GGCAGTGCCC CTGCCAGTTC TCCTAAACTT ATTGTTTACC CTGCCCTCTT CTTCCCCTGC 960
AAATTCAGAC AGCCAGGCGA TAGATTAGAT AAATAGATTC CATGTCCTTA CATTTGCAAC 1020
AGGCTTTCAT AGATTCCTTT GCTCTGGAAG GTGGCATCAT TATACAAAAG GACAAGTGAG 1080
AACACACGAA TGTAATCAGT GGCAGAACCC TGGGACTGAA CCCTACAGGA GTTCTAAGTC 1140
TATTGTTTCT CCTACCACTT CACAAATGTG TCAGAAAGAG CTGAATGAGG TGACCAGCTG 1200
CACCTGACGC TAGCTGGCTT TCGGAATGCT CAGGCCCTGG GCCCTTGGCT CACCACAACC 1260
ACTCTTAAAT TGACTAACAA TTGCCCCTTA GTGAGTGACC TCTCCAGCAA GCCCGGAGGA 1320
TTTTGCCCAG 1330
|
