| Tag | Content |
|---|
EnhancerAtlas ID | HS050-10461 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr10:127845080-127846890 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr10:127845372-127845387 | AATGTCAAGGTCAGG | + | 6.32 | | POU2F2 | MA0507.1 | chr10:127845976-127845989 | ATATGCAAATGTC | - | 6.19 | | RREB1 | MA0073.1 | chr10:127845588-127845608 | TGTGTGTGTGTGTGGGGGGG | - | 6.17 | | RREB1 | MA0073.1 | chr10:127845586-127845606 | TGTGTGTGTGTGTGTGGGGG | - | 6.95 | | ZNF263 | MA0528.1 | chr10:127846424-127846445 | AGAGGAAGAGGGGAAGGAGAG | + | 7.39 |
|
| | 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 |
| GH10I126157 | chr10 | 127845881 | 127846030 |
|
Enhancer Sequence | GGCCCCCTCA CACCCTGAGG AGCGTAATTT CATTTTCAAT AAATCTCTGC TTCTGTTGCT 60
TCATTCTTTC CTTGTTTTGT TTGTGCATTT TGTCCAATTC TTTGTTCAAA ACACCAAGAA 120
CCTGGACATC CTCCAGCAGT AACACTTCTG GGTGCGTGGA TGTGCTTTGG GTGGAGCATC 180
CTGCAAGGGA AAGGCTTTGC GTAGGGATCC GACAACTACT GGGCCCTAAC GATGGAGCAG 240
GAGTCGGCCA GGCCCAGGAC AGGGTGGAAG GAGAGGGGAA ATCCTGGCAG ATAATGTCAA 300
GGTCAGGGCC TGAAAGGCCT GGAGTCTGGG GAGCTGGGCT GGTGGAAGAC AGAGAAAGGC 360
TCTAAACAGA ACCTGGGTTT TCTGTGTCTG GACAACAGGG AGTCAAGAGT TGCTTTAAAT 420
ACTGAACTTT GTGGATGGTG AAGGTGCTGC CTGCCCTTTC CTGTCTTCAG AGGAAGACAC 480
TCTCCACTCT TCACACCGTT TGGTTTTGTG TGTGTGTGTG TGGGGGGGTG CTCCTCCACT 540
CTTGATCCAG AGATGAACAT GTGACCCAAG CTAAGCCCAT CACAAATCTT CCCTACAGCA 600
TGTTGAGCTG GGATGTCTGG GGATGACGTC TTTCTTCTCT GTTCTCAAGG CTCTGAGAAT 660
GTGGCCACCA CCTCCATCCT GGTCCCTTAC TTCAGGAGAA AGCTAGTCAG AGAGAACAAA 720
GCTGTCACCC TCAGGCAGGG ACAAAAGGCA GGGAGAGGGA GATGGACCTG TTGCCCATGG 780
GGCCTGCTCC GCCTCTCCTC CTCCTCATAA GTCCCTCTCT TCTGCCTACG CTGGCTGGAG 840
CTGGGTTTTG CAACCAGAGT CCTGATCAGT ATGGCAGGGA AGGAAAAGCA GCGGGAATAT 900
GCAAATGTCA GAGATGAGAA GCACTTCCTT ACACAGTCAG AGTTCTTAGA CCTGCTCCCA 960
GCCAAGTTCA GAACTGAGAG TCAGCTCCTT GTTTTACATG GATTGCAATA TGTTGAGGAT 1020
ATGCCTGGCT TAAATCAGTT AGACCCCGAT GGCAGGTCTC CGCTGCAGTC TACTTAACAG 1080
CGAGTGTTTG AGAGAGTGTG CGGAAAACAT AAAACACAGA CGGGCCCTCA CACTCACTGG 1140
CAAAGGCACG TGGGCCTCCC AAGTGCTGCC CCTCACTCTC CTCAGCAGTG CACATGTCGT 1200
GCCAGAGAAA GTTGCCCTCC TTGGCAGCGT TGAGCTCTGA AACCCCTGTC TTCTAAGCTC 1260
ACCTCCTCTG AGCTGCCAGA GGGGCTGCCT GGGCAGGCTC ATTCACAGGG CACCCTGGCC 1320
CTGTCACGCA GTCATGAGCA AAGGAGAGGA AGAGGGGAAG GAGAGCAGGC AAGGCAGTGG 1380
GAAGGTGACA GGGCCCTGAA GAGAAGAGTG TGAAGAAGGG GTAGTCCTTA GTCATAGGTA 1440
GAGAGCTCCA GGATGGTGGA GGAGTCTGGT GACCTTGACA ATGGAGATGC AGCAGGTGAG 1500
CCCAGGTCAA GGTGACAGGC GAGGTGAACG AATGTTCCAC AGCACAGTTC CAAAGGGAAG 1560
CAGAGAGGCG GGATGTGAAA ACCAGAGACG GGGACTTGAG GGGAATAACT GGAGGGATGG 1620
GGCTGAGAGG GGACATGGGT GAAGCTGCAG AGGAACAGGC AGAAGGATGC AGAGCACAGA 1680
GGGATACACA CAACACAGGA CATATCTGCA GAGCACGGGG TAATGCACAC AGCACGGGAG 1740
AAAGCACAGA GCACAGGGAG AGAATGCACA GAGCACCGGG AGAGGAGGCA CAGAGCACAG 1800
GGGGAGGCAC 1810
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