Tag | Content |
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EnhancerAtlas ID | HS050-50250 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr4:1993680-1995050 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr4:1994421-1994440 | CGCCGCCTCCTGGTGGCCT | - | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 1993721 | 1993761 | chr4 | 1993863 | 1994061 |
| | Number: 1 | ID | Chromosome | Start | End |
GH04I001992 | chr4 | 1993886 | 1995010 |
| Enhancer Sequence | CAGCCTCCCA CCTCCCAGCA GCACCCAGTC CACTGGGCCT ACTCTTCCAC CGGTGCGCAG 60 ATGCAAGAAA ACCTGAAGGG TGAGAAGCCG GGGCCACCAC TGCTCCCGCA GAAAGCCTGC 120 GGGTGGGAAA TCCTGGGGAT GAGGGGCGTA GAGCAGGCAG GTGCCCGGCA CAGCAGAGCG 180 CAGGAGCAGG GTGGAGTCAC CTGCCGCGGG GGTGTGTGCC TGGGCAGCAG GGGGTGGGGC 240 CTGGGACCTG GGGCAGCACC CGTGACAGCT GAGCTGGTGC CTAGTCACCA TCTAGGCAGG 300 GACGGCTGCC TCTGGGTCTG GACGGCGCTG GGAGTTGGCG CTCGTGGAGC CTGGAGGTGG 360 CCCCGGGATC TGGAGTGAGG CCAGGGCCTT GGGGAGGCCA TGGGCGACGT GCGTGGAGGA 420 AGCAGGCGCA CCCCGTGCTC CCTCAATACC TGGGAGGCCA GATCCATCCA CACCAGGGCC 480 TGCTTCGGCC ACATAAACCC CCTCCCACGA GGAAACGCAG AGAGCCAGGC CATGGCGTGC 540 CTGTGCCTCT GCCATGCGCC CACTGGGCTG CTCACAGTGT GAGACAGCTG GGCTGGCTGG 600 CGCTGGGGGT GAACAACAGC GCCCTGCCCT GTCCAGACGC CGGGGCTGAA ACCCCAGCCC 660 CAGGCCTTCC TGACACCCAC TCCCTGCGTC AGGCGCCAGA GACCCGTCCT ACGAGGGCTG 720 CGGCCATCAC GTCCCCGCGA GCGCCGCCTC CTGGTGGCCT CTGAGTGGGA GGACCTTCCA 780 GCGCTTCCCT CACTGTCCTC ATGGGCTTCC TGCCCTGAGG GAAGTTGGCT CGAAGGGCAG 840 AGATCAGAGG TCGTGCCAGG GGAGCCTGCC TGCTGCCAAG CCCCTCTGCA TCTGCCCTGC 900 AGGACACCCA GCTGCCCTCA GGAGTCAAGA ACCCCCCGCG TGGCCCAGCC CCTTCTGTTC 960 CTTGGGCAAC CAGGGAGGGT GTCGCCCCGG CCGCTGACCC TGCGCCCCGG GCCCTCACTC 1020 CCGACGCCCG CCCGAGCTGA GTGCGCGATG CGGCAGAAGA TGCTACGTGG CTGCAGGAAG 1080 CGCTGCGCAC ACGCTGCCTC TGGCAGCCGC ACAGCCCGGC TGTTTCCAGC CAGTGCGGCC 1140 TCTCCACAGC AGCCCCAGGG AAACCCTACG CCTGCCAAGA GGCAAGCGCG CGGCATTTTA 1200 TAAAAATGGT AAGGATAAAA AAAGTCGGGG ATGTTAATTT AAAACAAAAA GGACCACTGT 1260 TGTGGAGTCA ATGTTTTCTC TCCAGAACGC GCATGTTGAA GCCTGGCTCG CTCTACTGGG 1320 GCTTCTTGTA GGAAAACGCT TGGCTTTCCC GGGCGCGGTA GCTCATGTCT 1370
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