Tag | Content |
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EnhancerAtlas ID | HS050-13107 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr11:76032310-76033870 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr11:76033131-76033142 | GGGCGGGAAGC | + | 6.02 | ZNF263 | MA0528.1 | chr11:76032410-76032431 | GGAGGAGGGTTGGCAGGAGGG | + | 7.26 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CGTTCTGAGA CCCTGAGGGA GCAGGGAAGA CTTCCTGGAG GTGGTGAGTG GGGCACTGAG 60 AGAGGCCTTG GAAGAGGGTC CAAGCTGGAC TAACGAGGAA GGAGGAGGGT TGGCAGGAGG 120 GAGACATTCC CACTCCCGTC ACCTGGGTGC AGGCACTGTG ACTTCTGCCT ACAGCCTCCT 180 CACCCATCCC CTGCCACTCC CCCAGTCCCC CCCCGCCCCC CCCCGACACC AGCCAGAGTG 240 GCCTTCCCGG AAAGCAAATG ACTGGCCAGT CAGGGTCCTG CTTACAATCC CTCAGAGTCG 300 CCCATCCTCC AGCATGGTTT GCCAAGGACC TGCTCGGGAC TGGCTCTCCC CACTCTCTCC 360 AGCCCCATCT TGAGCCACTA CACCTTGAAT TCAGCGTTTC AACAACACAC AGTATTTGGA 420 ATTTCTCCAA CTGCCCCCCT GTTGGTCTTT GCATATTCTG TTCCCTCTGT CCATCATATC 480 CGTTCATCTT TCAGAGCTTA GCTGAAATCC CTCCAGGACG CCTTCCCTGA GCCCCGGATT 540 GAGTGGGGTG CCCTCCCCCA GCTCCCACCC TGGGTCTGTG TCTGCCTGCC CTGCCCATGC 600 CCGCCCCACA AGGCCCACGC TTGCGCCCTC GGGCTGCGCA GGGCGAGGGT TTGGGGGCGC 660 GGTACTGACG GGTGTCCAGG CCTCTCCTCG AAGGGTTCCG CGCGCAGAAA GGTGGGCCGG 720 GGCCAGAAGA CGCGCTGGAA AGGCGTTTTC TGCCCCCTCC GGGCCTCGGG AATATTTGTG 780 GGCTGCCGGC GGGGCAGGCG GGGTGGGGGA GGCTGCCCGG CGGGCGGGAA GCCCCGCGCA 840 CTCGGGTCCC CTGCGGTCCC CGGCGGGGGT CGGCGCGTGC GGAAAGCGGC CCGAGCCCCC 900 AACCTCGGCC CGTCCGCAAC CGAAGAGGAG GCGACCGCAG CCTGGAAAAG AAGAGCCCCC 960 AGCTGTTTCC TTCCACCCGG GCGGGCGGGA CGGAGAAGGG AGGGAGCCTG GGAGAGACGC 1020 AGGTGTGGCG CTCGCCTGTG CTGGCGGGGT GGCAGCCGGG GCGTGGCACC CTCGGAGTCT 1080 CGACTCTGCC CACTTCTCAG GCAGAAAACT GAGGTGGTCC CATGGCCAGA GCTAAGAAAG 1140 GCAGTGCTGA TTCCTGGGCC CCCGCTGCTC ACAGCGTCCT TCAGCATCCC AGTAGGCCGA 1200 GGGCATCTCA CTCTTAGGTG ACCACAAGAA TCACGGGGAC AGTTGTTAAA ATGCAGATTT 1260 CAAGGCCCCA TCTCCCAGAG ACGCAGTAGG TCTGAGATGG GACCCAGAAA TCAGCTCTTT 1320 AAAACAAGGA AATAGTCCAC ATGTTGTGAA GCACTGGTGA AGAGATGCTT TGGAATAGGA 1380 AGCTTCCCCC TCGGCCTAGT TACAGCAGAG AGCAGAGAGC GAGGACTCGG AAGGGAGGGA 1440 CTTGGACCCT GAAGCCCAGG CTTTCCTGCT GGGTGACTAA CTTCTCTGTG TCTTGATTTT 1500 ATCTTGCCTA AAGTGGAGAT AACATTCAGC CCACAAGGTT CTGTAAAATC AAAGAGATGT 1560
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