Tag | Content |
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EnhancerAtlas ID | HS050-19654 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr13:113676610-113678120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr13:113677596-113677610 | AGATAATGAGTCAT | + | 6.03 | NR2C2 | MA0504.1 | chr13:113677284-113677299 | CGGGGGCAGAGGTCA | + | 7.3 | NR2F1 | MA0017.2 | chr13:113677290-113677303 | CAGAGGTCAAGAG | + | 7.04 | ZNF263 | MA0528.1 | chr13:113677532-113677553 | GAAGGAGCGAGGGAGAAAAGA | + | 6.15 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_05825 | chr13:113676920-113678360 | Brain_Hippocampus_Middle |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH13I113021 | chr13 | 113676043 | 113678502 |
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Enhancer Sequence | ATGAGGGGAT CTTGTTGCAT CCGCTCCTCT TCCTAGCTGG GCCCTCCACA GCCAGTGTAC 60 CCCAAGGAGC AGCTTCTCCC TCCCACCCAC CCCCGCCGGC CAGGGGTCCT CATGCCGTGG 120 CCCATGCCCA TTTGCACAGG GACGCAGGGG GTCTCACACA CAGGCAGGGT CCGCCCCCAG 180 CTGCCGTCGG CGTCACTCCA CACACATAGG CTTCTGGGCG GTGCTGGAAG CTTCTGGCCC 240 CTGAACGTTC CCCCCAGGCC CCGTTTCAGG GAAAGGAAAG GCAGGCGCAG GCTGCGGCCG 300 TTTCCACAAT CCACCTCGTA GCTGGGGCGT GCCGCTTGCC TCGGCTTGTC CCGGCAGAAC 360 ACTCTTACCT TTAATGGCGA CTGAAAAGTT GCCACGAGTT CCTGATCATT GTGGTAGGTG 420 CTGCGTGAAG CTGAGACGTG CGTGAGCCAC ATCCCAGGGG GCTTTGAGCC CCCACCGCGG 480 CGGCGGCTGA GGGGAGGCTT GTCGTACTCG CACAGGAGGA CACAGGGCTG CAGTGTTCAC 540 TCCAGGGCCT CTTATCATTG GGATCTGAGG AATTTTCCGA GAGGAAGTGC GAATTAACAA 600 TGATGAAAGG TTTGTGAGTG AGTGACAGGC ACGTTCTATT GAGCACTGCA TGGGGCATTA 660 TGTGCCACCA GAGACGGGGG CAGAGGTCAA GAGCCCTCGA GGGCTGGGAG AGTTCGGAGG 720 ATAGAAGTCA TCAGAGCACA ATGAAGCCAG ACCCTGCAGC CGCCTTCCCC TTCGGGGGCT 780 TCCTTAGAAT GCAGCATTGC GGGGACTGAG CTGTCCCAGG TGAAGGGGGG CCGTCACGGT 840 GTGTGGACGC CCCTCGGCTC AGCCCTCTAA GAGACTCGGC AGCCAGGATG GGCTCAAGGC 900 ATGAGCCCTC AAAGGAGGTT AGGAAGGAGC GAGGGAGAAA AGATATGCTT GTGTGACGTC 960 CTGGCCGAAG TGAGAACAAT TGTATCAGAT AATGAGTCAT GTCCCATTGA GGGGTGCCGA 1020 CAAGGACTCG GGAGGAGGCC ACGGAGCCCT GTACTGAGGA GACGCCCACA GGGAGCCTCG 1080 GGGGCCCAGC GTCCCGGGAT CACTGGATGG TAAAGCCGCC CTGCCTGGCG TGGCTGGGCT 1140 TGGCCAAGAC CCAGAAGCAG AAGTTCCGGA AGCTGGAGAC AGTGGCTGTG GGGGGCGCAA 1200 GGCGGCGGGG GACTGTCGCT GTTACGAGAC AAAGCTGCAG TTGTCGGAGG CTGTGTGCAC 1260 CCTGGGTCTT CTCAGTGAGG ACGTGGATGA GGGGCGGCGA ACCCACCATT ATCTGTTCTC 1320 CATAAAAAGC TACCCTAAAC TTAGTTAGCT TGAAAAGCCC TATTTTACAG ATTTATTCTT 1380 CATTTAGTGG CTCAGAAGTT CCAAAAGGGC TCAGCCAGGT GGTTCTTCAC TCCACGCACG 1440 GGGCACTGAC TGTGTCCTCT GCTCAGCTGT GTCCTCATGG GGGCTGGGCT GGAAGGTCCT 1500 GGGGGCTGCA 1510
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