Tag | Content |
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EnhancerAtlas ID | HS050-10653 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr10:134111110-134112370 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PLAG1 | MA0163.1 | chr10:134111884-134111898 | GGGGCCCAGTGGGG | + | 6.36 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 134111134 | 134111482 | chr10 | 134111558 | 134111896 |
| Enhancer Sequence | TGGAGATAAA ACATCACTTC AGACACACAA GATGACTGAT GTTTACAAGA AAAAGGAAAA 60 AGAATTGGGG GCAAAATAAA CAAAGACCCT GGCAGTCACA GGTGCGTCCT CCAGGGGCAG 120 TGCAGGAAGC CCTGAGCCAG AGCTCCGAGA CTCCCCGGCG AAGCCCCCGT AGTCAGGGGC 180 CCGCCCCGCG GCCAGCAGCA GGTGCACACC CGCCTGGTCT CTGGGGCTTT ATTTTCCAAA 240 CTCAGGAAGA TGTTGACTCC ACTCCAACTT CCTGTTTGTT TGTTCTCAAG TACAAACAGC 300 CTTCCCTCCA AGCTCTTTCA GTTTCAAAGC TCAGAAGATG CTTTGTGTCT CCTGGGGTCT 360 TGGTGCTCTG CGGCAGCAAC CCGGGTACAC TGGCTGGTGC TTGGCCATTT GGCTAAACTG 420 GGGTTAGAGG TGGCTGAGAG AGAACTTGTG TGATGCTGGC AGGTGGCAGG CAGCAGCACC 480 ACTCCCTGAA GGTCACGCTT CCAACTCGTC CCTGCTCTCC CGGCCCCATG TCCAGCTCTT 540 CCAAACAGCC CGGCCGACCC GCAGCAGCCC TAGCCCACCC CCAGATGCGG AGACTTCACC 600 CTGTGTGGTC CCTCCCCTGA ATCTGAGCTG GGCCTGTGAC TGGCTCCAAC CAGCAGAAAG 660 CAGTCAAAGT GACACGGTGC CAGCCCAGGC CTAAGCCTCA AGAAGGCCCG GCATCTTCTA 720 CTCTGCGTCT GTGGGCGCCC TGGGGCCTCT CAGGAATTCC TCCTGCCCCA ATGTGGGGCC 780 CAGTGGGGCG AAGAAGCCGA GACTCTGAGG ACGGCTGTGG TGGTGTGAGA CAAGTCCACA 840 GGTCCCACGG CAGCCCCTTC CGATGCGGGG TCCAGCTCCC CTCCCCTGAG GATGAGCTGG 900 ACTTGCTCAC TTGCTCCTAA CAGGACATGC TGGGAGGAGC CTGTGGCTGA GATCCTCGCT 960 GTGGCTTCTC GCTCCTGCTC AGCTCACTGG GGAGGGAGGG AGGGGAGCGC CCTGTGTGGG 1020 GTCACCGGGG AGTTGAGCGC CGTGTGTGGG GTCACTGGGG GGGAGTTGAG CGCCGTGTGT 1080 GGGGTCACTG GGAGGGAGTT GAGCGCAGTG TGTGGAGTCA CCCAGGCAGT GTGTGGGGAA 1140 GCTCCCTTTG CAAGGAACAG AGGCCTCCAT CCAGGAGCCA CATGGGGAAG CTGGCCTGGA 1200 AGTGGTCGCT CCAGTCCCAG TCAAACCTTC AGGTGACAGC AGCCCCAGCT GCCATCTTCA 1260
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