Tag | Content |
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EnhancerAtlas ID | HS050-32613 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr19:5581430-5582630 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr19:5581561-5581572 | AATAAACAATG | - | 6.02 | GLI2 | MA0734.2 | chr19:5582021-5582036 | AGACCACCCAGGAAG | + | 6.26 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | CACCCTCCCA AAGTGCTGGG ATTACAGGCA TGAGCCACCG CGCCCGGCCA AAACCTGTAT 60 TTTAAAAGGC TGTGCACTGG GGAGATGCAG ATGCCTGCCC CAACGATGCT TATGTGGTGG 120 AGAGTGCCGA CAATAAACAA TGCTTTAGCG AGTGGTCAGA GCCACGAGGA CAGGCAGGTG 180 TGACAAGGCA GAGGGTGATG AGGCGCTGCT GATCCAGTGG TCAGAGGAGA CCTCTTGCAG 240 GGGGCAGAAT TTGAAGGGGC TGGGCATGTG TGGCTGGTCT CCTCAGTCAC AGCCAGTGCC 300 ACGCTGTTCT TTTTTGAGAC AGCCCTGTCG CCCAGGCTGG AGTGCAGTGG TGTGATCACA 360 GCTCACTGCA GCCTCTGCCT CCTGAGCCCA AGTGATCCTC CCTCCTCAGC CTCGTGGGTA 420 GCTGGGACTA CAGGTGTACA CCAGCAGCCC AGCCAATTTT ATTTTTTTGT ACAGATGGGG 480 TCTTGCTACA TTACCCACAC TGCTCTCAAA CTCCTGGGCT CCAGTGATCC TCCCACCTCA 540 GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCACCGGG CCCTGGTTCA CAGACCACCC 600 AGGAAGCTCT CCCAGGAGGG CAATGTCTCG GGTCCTCAGT ACCTTATGCT CCACTGAACC 660 CGGCAGCTGC TGTGTCAATA TTTGCAGGTG GAGGCAAACA CAGGGCAGCT GCATCTCACG 720 AGGATTTGAG GAGTACGGAG AAGCGGCTCT TGGTGCTCCC GGGAGTAATT TAGGGGCAGT 780 TTCTGGCCCA GTATTGCTGT CTCTGGAAGC ACTGTAGGAC ATGTAGAGTT ATCCTTGGGG 840 TCAACTCTAA AGGCCAAGCG CATGTGCAAA ATTATGTACA CACTCACGTA CGCAGCTTGC 900 TCACTGGTGC CCCAAACACC TATCCCTTCA CCACCGTGTG ACCGCGGCAC GGGGTGCCCT 960 GACAACCGGG GAGGCTGAGG AGAAGGGACC TCGGGCTGCA GCCTCAGCTC CATGGCTCGC 1020 TACCTCTGGG CGGGTCTCAG CCTCCCTCGG GCTCAGAACC TTCTTCTGCG CTTGACTTTC 1080 CCAGGAATTG ACTCCAGTTT CCCAGGGAGC TGCACTGGGC TATGTCTGGG TTTGGTGATG 1140 TTGTGTGGCG TCCGTAGGTG TCCTCATATA AATTGGTGGC TGGCCAGGGG GACTAGAGAT 1200
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