Tag | Content |
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EnhancerAtlas ID | HS050-49791 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr3:186130910-186132390 |
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) |
MAX | MA0058.3 | chr3:186130978-186130988 | ACCACGTGCT | + | 6.02 | MEF2A | MA0052.3 | chr3:186131764-186131776 | GCTATTTTTAGT | - | 6.18 | MEF2B | MA0660.1 | chr3:186131764-186131776 | GCTATTTTTAGT | - | 6.62 | MEF2C | MA0497.1 | chr3:186131763-186131778 | GGCTATTTTTAGTTC | - | 6.41 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 186131140 | 186131200 | chr3 | 186131407 | 186132227 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I186413 | chr3 | 186131314 | 186133044 |
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Enhancer Sequence | TAGAGAAGTT GGGTCACCTG CAAGCGGCAT AAGGCAGGCT GTGAACCCAG GTCTGCCTGA 60 TTCCAAAAAC CACGTGCTCT TAACCACTGT ACTCCATTAC CATGTGTGGA GTGCCTACTG 120 GGTGCCAAAA TATAGCATAA GACAGAAGCA GCCAAGGCCA TTCCCGGGGA CCCCAGACCC 180 CAAGGGAAAT GCCTTCCTTC CCCCCAGCCC CTGGAGATGT CCTTGGCTGC CTCCTTCTCA 240 CTGTGCTCTT GACCTTGGCT ACTCTTGGGC AGTACCCAAA AGACCCAGGG AACACACTTC 300 CCCTATTCCA TGTCTCTCAG GACAAATGAG GAATTACAAA TAAACCGTAT TAATTCATCT 360 GTGAACTCCA AGCCTCTGGC ACAGTACCCG GCAATATTTT ACATGGTATA TAGCACCTAA 420 CAGGCTATAT TCAAAAAATA TCAGAAGATA GACGGGAGGA GACGGTCACC ATGCCAGGCA 480 GGGAATGTTT CCAGGGAGAA CTGTAGCTGC AGGGAGTGGG ACTTATCCTG ACTGCCCTGG 540 GAGATCGCTA ATTTAGAGCA CACCAGTGTG ACAGTACATT TCTTTTGAAA TGCAACTCAA 600 AATCCGCTTC CTCCAGGAGG AATGCCAAGT GGCGTCCCGG AACAGGACAA GTTGTACTTC 660 ACAGGAGATG GGAAGCTAGA GGGGGGAAAT GCCATCATTA ATCCACCAAG CAGCAGGGGG 720 TGGGGGCGCT TGCCTCCAAC AGGCATGGCT GGAAAAATAA GCAGCTCTGG CTTGTGCTCC 780 TCCCTGTGTC CCTGCCACGA CTGTGAAGGG CTAAGAACAC AGCAGAAAAG GTTCCAGTTC 840 ATTTACAAGC CTCGGCTATT TTTAGTTCAT CGATCCCTGG GCGCGGTGTG TGTGTGTTGA 900 GGGGGGCCGG GGGACGGGGC TTGCAGAGCT CACGGTTTGA GGTGGAAGCT GGGGAAAGCT 960 TTAGAATTCT TTTCATAGAA CAGGTACTCT GTTCACTACG CACCATCCAG CCTCTGGAGA 1020 CCTAACCGCT TTTCTTGGGG CAGGAAGAAG GAGCAGTGTC AGGGGAGGGA GGAGACTGAA 1080 ATGAGAAAGG GAACGAGGCA AGAGGCGGTG ACGCCCTTGT GCCAATGACC AAATTGGGTC 1140 AGAAAGAACA ACCTTTTGAA TGCAAGTCAG GAAATGTGAA TCGCTGCCTC AGCAGGGCCA 1200 GGTGCATGCC TAGTGGGTGC CGGCCCAGCC TGACCAGGGA ACTGTGACTG TACCTCCTGC 1260 CGCTCTAGAG AACCAGACCG ATGACCATCT AGAAGTGCAC TGATCTTTAT TCCTTGCCTG 1320 GTGCCCTGTG GCCAGTTCAA TTCCTATTAT CAACCCCTCC TTAAAGCTGT CAGGGAAAAG 1380 GAAGGAGAAG TTCACATTTA AAGATGGATC TAAATGGTGA AAGAGGTGAA AATCATTGCC 1440 TTAAAAGAGA TCACCTGTGG ATTTTGTGAG TTATTAATTC 1480
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