| Tag | Content |
|---|
EnhancerAtlas ID | HS050-69693 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:107730110-107731720 |
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 | ATACAAAAAT TAGCTGGGTG GTAGTGGCAC GCGCCTGTAA TACCAGCTAC TTGGGAGGCT 60
GAAGCAGGAG ACTCTCTTGA GCCTGGGAGG CAGAGGTTGC GGTGAGCCGA GATCGCGCCA 120
CTGCACTCCA GCCTGGGCAA CAGGGTGAGA CTACGTCTCA AAAAAAAAAA AAAAAAAAAA 180
AAAAAAGAAG AAGAAATTTA ACATACAGGC GATTTTTCAG GTTCTCATTT GCTAAACCAA 240
CAATGCAGAA TTTGTGAAGT AGGGGCAACA AGTTGCTGAA CCTGAGAGAC GCCTCTAAAT 300
GCGCTCAGAG GTTATTTCAA CTGTGCTGTT TGCTAGTTCA GGTACAACAG GCAAGACAGA 360
AAGATGCCAC CGCTCTCTCC ACCCTCCCAG CGCCGGATCA CAGAGCGCAG ACCATGCACC 420
CAGCCTTCCA CACACGTCGC GATCTCGCCG CTTTAAGCTG CTGGGTACCC TCGGCCCGCC 480
CACAAGAAGG CGGGGCGGCG CGGGGTCTGC TGGGAGTTGT AGTTTCGGGC CGGGCCCGAG 540
AGCTTCTTGA CTCGTTTCCT TCTACCCCCA CCGCCGCACA GCTGCCTATG GACTCTGGAG 600
TTGCTGTGTA TTGAGCATGG GGCACAGCCG GGGGTAAAAG GGGAGAAGGC TCCTTTAATC 660
TGCGGATCGG GGCGCCGTTG ATGAGTGTTA GAGGTGTTGG AACGCAGAGT AAGCGGCGCG 720
CATGCGCGGC TGCCGGAGGT GGGGGCCGCT CCTCCCGTGC CACTCAGGGG CTGGCTGCTG 780
CCTTAGGGCT GACTGGGCTC ATAGGTAGGG CCTGCGGTGC AAGTTTGTGA TAACACTGCC 840
TGTAGGCTGC GGTTGTTAAG GCAGAGATTT GAAGGGGGTC GGTTGGGGGT GCTGGGTAGT 900
GTCAGTAATC AAGGGTTTTA ATCGCTACTC CATCCTGGCT TTCGGGAACC TCCCACCTCC 960
TACCCTTTCC CAGTTTGCAG AATTGCAGCT TTCCCCATCC CCCACCCCGA TCGCTTCGTG 1020
GGAAGCCTTT CCATACTGTG TTGTGAAATC CGTTAGACCT CAGCCAAGGC CTTTTAGCCC 1080
GCCCGGAATT CAAGCTGCCC CCTCCTTGCC AAATCCAGAT CATGCGAGAC AACAAAAGGC 1140
TTGAGGCACA AGCCCTACAA GGCAGTGCCC CTGCCAGTTC TCCTAAACTT ATTGTTTACC 1200
CTGCCCTCTT CTTCCCCTGC AAATTCAGAC AGCCAGGCGA TAGATTAGAT AAATAGATTC 1260
CATGTCCTTA CATTTGCAAC AGGCTTTCAT AGATTCCTTT GCTCTGGAAG GTGGCATCAT 1320
TATACAAAAG GACAAGTGAG AACACACGAA TGTAATCAGT GGCAGAACCC TGGGACTGAA 1380
CCCTACAGGA GTTCTAAGTC TATTGTTTCT CCTACCACTT CACAAATGTG TCAGAAAGAG 1440
CTGAATGAGG TGACCAGCTG CACCTGACGC TAGCTGGCTT TCGGAATGCT CAGGCCCTGG 1500
GCCCTTGGCT CACCACAACC ACTCTTAAAT TGACTAACAA TTGCCCCTTA GTGAGTGACC 1560
TCTCCAGCAA GCCCGGAGGA TTTTGCCCAG GGTAATGTTT CACATTGAGC 1610
|
