| Tag | Content |
|---|
EnhancerAtlas ID | HS050-01757 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:36947290-36948410 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:36947683-36947704 | GAGGGAGGAGGGGGCTGGGAA | + | 6.37 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCAGCTCAC AGAATCCAGC ACAGTTCAGT TTTCCCCTCA CCCCTGCCTC CCTCACAGCC 60
TGTGTGGTCA CACCTCCCAG GACTGCCACC TTGCTTTTGT CTGTGCCACA CTGCGCAGTT 120
CCAAAGCCCC CTTTCTGGAT CCTCTCCTCC TAACTCCTGG GCCCCCTGGC CCTCCTGTCA 180
CTGCGGCCAT CTCTGCTGGG CTCTGCAGGT GCTCACTCCT GTGGCCCAGC ACAGCTCGAT 240
GTCTCCTGGG CTGGCTGCCT TCACATTCCC TCTTTCTGTT TCTCCCTCAT CACGCTCAGC 300
CCTCTCCCCT CACACTCTCT TCCCCACTTC ACACCCCTCG CTCCCTTGCT GTTTCTACTC 360
TCACCTCGAG ATTCTTTCTG TGGGAAGGGT GGGGAGGGAG GAGGGGGCTG GGAATAAACA 420
GAGGGGAGAG GCATTTCCAG ATATGCTGCA GATAAAGAAA AAGAGAGAGC AACAGGAAGA 480
GTGACAGAGT GAGGCGGTGA CTGAAATCCA CACAGACTGA AACGACAGAG AGACTCGCCA 540
AGAGGACGAT TGAGGCCAGA GAGATATCGA GAGACAGAGA AAAAGGGCCC AATGTACGCC 600
GACCCAGAGA GTGGGCGGGG GGGGGGCACT CGGAGGCCTG GAGCCCGGGA AGCGTCTGTT 660
ACCGAGAGTT TAAGATTCAA GAGATAGCAG GAAATATGCG AGACAGAGAA ACTCAGAGAG 720
ATAGCAAGCC AGAGAGAAGC TGAGGAGGAA AGATGGAAAC AGAGAGTGAA ATAGAGACCC 780
AGACGGGGAG GGGTTGCGCG GCTGGAACTC ACAGACACAC ACGTCCTGAG AGACAGAGGC 840
ATGGGGAGGG GAGAATGATT ATGCCTGTCC CCAGCCCAGC TCAGTGTCCC CAAGGAGATA 900
CTTGGCTGTG AGTGACTTCC CTGGTGCAAT ACCCCCAAAA GTAGGGGCAT CCTGTGAAAA 960
GAGACTCAGT GTCCAGGGCT GGGGTTCCAA AGGACGAATC CCGGGCCCCA GGCCTAGGAC 1020
CCCGGACATG AACACTTGGC AGAGCTGTGG GGAGTGGCCC CAGGATTCCA GCTCTCCATC 1080
AAGCCCAAGG CTCAGCCCCT CTCTAGGGAT CCCCTACTCA 1120
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