Tag | Content |
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EnhancerAtlas ID | HS050-24723 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr16:1958350-1960490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr16:1959788-1959800 | CAGCACGTGGCC | - | 6.37 | Myod1 | MA0499.1 | chr16:1958685-1958698 | AGCAGCTGCCCCT | + | 6.18 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 1959283 | 1959736 | chr16 | 1959743 | 1960198 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I001909 | chr16 | 1959861 | 1960010 |
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Enhancer Sequence | TGATGACTCT CCCAGGGAGC GCCTCCCTGC ACGCAGCCCG TAGGTCCCCA CCGACATCTG 60 CCCTCCGTGT GTTCGGAGGC CCAGCTGGGC ACCTCACCCG CATTGAGTGC TGGTGGTTAG 120 GCGGAGTTCC TGCTCAGCGG GTGCAGAATA CGCCAGCCCA CCCCTCGCTG CTTCCAGAGT 180 CTGCCCCCCC AGGCCCTGGG TTCAGGCCCC AAAGCCAGCC AAACCAGTGC CCCACCCCTC 240 ACAGCTCTGT GTCGGGACGG AAACAATGGG GTCATTTGGT GGACTCAGAA AAGGAACTCT 300 AAACGGAGGG AGGAAAGTAG CAGAGCCTCA GTGAGAGCAG CTGCCCCTCC ATCCCGTCAG 360 CACCTTCTGC AGGGAAAGGC ATTCCAGACA GAGGGAATAG CACATGCAAA GCCCATGAGG 420 TTGGACAGGC CACGGCAGGT GGAAGGAGCT GGCAGGTGCC AGTGTGGTGG GCGTGCTGGA 480 ATAAGGAGCG CATGTAGGAC GGAGGGGCAA GCCGTAGAGG GCTGTAACAG CTGTGATCTG 540 GAGTTTGGTT TTCATCCTAG AAGCAATAAG GGGAAAAGGT GGGGATCAGA GAGTTTTAAA 600 ACAATAGGAT CTGGTTTATT CCGCGACGGC CCTCCAGCTG CCATGCGGAG AGCTCACTGT 660 AGAACAAAAG AGGTGGTGGG ATGATGGTGA GCAGCCCCTG AAACGGCCCA GGCATGAGAA 720 GGGTGTGTCC AGGAAGAAGA AATCCACATG CACCGGGCTG GGAACTGGGT CACCAGGGGC 780 CAGGGGCTGT CCTGTATTCC TTCCCACCCC CAGGCCTGGG GCAGGCAGTT GGCCCGGTCT 840 TCACAGAGGG CACCCGTGCA GGGGGTGGGG ACAGAGCAGC CCAGCCCAGT GATCCCCTCC 900 TGGCAGGGAT CCGAGGTGGA GTCTGTTCCC TCTTCCCAAA GCTGCTGTCA GTCGGGGGGG 960 CCCTTTCCCC TCCACCCACA TCAGAGCTTC GAGGTAGGAC GGAGGCTGTG CCTGTGACTT 1020 GTCCACATCT GGGCCCACAT CTGCCCACCA TGTTGCCACT GCAGTCTCTG GGTGGGTGCT 1080 CGGAGGGGAG CTCAGAACCG GCCTCCAGCC CTGCCTCTGT CCTGGCCTGG GATGGAGAGG 1140 CCTGTGGGAA GTGCCTGCCC CTCAGGGCAG CTGCAGAGCA GAGTGTCCAC TGGGCCCAGA 1200 AACTAGCAGG AGGCGGGGTG GGTGTCCAGA CGCAGCCCCT CCTGCAAATC CTTCCTCACT 1260 GCCTGCATTC CCAAAACAGG GAGTGGCTCC AAGTAGCTGA GAGGCAGAAA GACCATATCA 1320 GGGCCTGTGG GACTCAGCGG GGCTGTGGAG ACCACAGCTA GGCCTTGCGA CAGACCTGGG 1380 GCTAAGCCCA AGCAGCCCCG GAGGTCATCG TCAGGGCAGC TGGTGGGCAC CTGGCAGACA 1440 GCACGTGGCC ACAAGCAGGT GAGGGTCATT ACTGAGGAGT CCCTCCTACT CCCAGGACAC 1500 AGGGGCGGAC AGGGCACCCC AGCCTGCCTG AGTCTGGCCT CAGTTATGAG CGGGCAGCTG 1560 GACTGCAGAT GGCCACTGAT CCCAGCCCTA TCCCCAGGGG AGGGCACAGA ACAAATACCA 1620 CGGAACTGGG GCAGCAGGGG CCTGGGGGAG TGGGTGGGGC CAGAGAGTGG GTGGTGCCTG 1680 AATGGGTGGG CCTCTACAGG GAAGGCTAAG AGGCTATTAA TCCGTCTCCC TGTGCACACA 1740 CCCAACACTC GCTGACCTCA CCAACACTCA GGCAATTCCA CAAGGCTCCA GAAGGAAGCG 1800 TCCACTGCGC ACCTGGATTC CGGATGAGCC AAGGTGGTGG GTGCGGACCC GACTTTAATC 1860 CTGCCCCACC ACTCCACAGC GAGGCCTGCA GCCTCACTTT CCTCATCCTG AACATGAGGA 1920 CAGCCCTGCC CAGCCTCCCA GGGCTGAGAA GAGAGCCTGA GCATGGCCCC CAGCATCACT 1980 AGGGCTAAGC TGCATGTCGC TGGGCGGGCC CTACGCCTCT CCGAGCTCAC AGGCTAGACC 2040 TGACCAGGCG CACTGCCCAC CTCTGAGGGT GTATAAAGAA TGAGTTTTGG GCCAGGTGTG 2100 GTGGCTCCTG CCTGTAATCC CAGCACTTTG GGAAGCCAAG 2140
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