Tag | Content |
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EnhancerAtlas ID | HS043-29544 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr3:119527770-119528900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr3:119528407-119528428 | GGGGGAAGGCGGGGGGGTGGG | + | 6.01 | ZNF263 | MA0528.1 | chr3:119528395-119528416 | GGGGGAAGGCGGGGGGGAAGG | + | 6.77 |
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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 |
GH03I119809 | chr3 | 119528119 | 119529647 |
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Enhancer Sequence | CAGAGTTTTC TTACCCAGGC CAGTTGGGAA GGCAAAAGGC AGGGATGGCA TCTGTGAAGA 60 ACATGCCCCT GGGCTGGTCA CTGGTCCGAG GCCCGAGGCC TCCAAGCTCA AACCTGCCAG 120 GTCACTGCGG GCTTGGCTCA GCTTCCCAGG CCTGCCCTCG GGGACCTCTG CAGCCCTACC 180 TGGCTGTTCC ATGCTCCTGG GCCAGCCTTC CCTCAGTTTC CACTCTGGAC CAGAATCAGA 240 GGCCAGAGCC AAGGGAGAGA TTGTTTCTTT CCATCCAGCT GTGGAGATGG GGAAAGTAAA 300 GGTAGGACTG CACTGACCGT GTCTTTTGTG GGACAGGCAG GACTTCCGGG CTGGGAGGAG 360 GAGATCTTGT ACCAGAGTCT CCAAAAGGCA TCTGCCCCAT TGCCTCTCTG CGCACCGCAG 420 AGAGGGGTGT GCGGGCCCGT GGGTCCCGCC TGCACGCTCT GCTGTTCCAG GCGCTCGACC 480 TCTTTGCCCC CTAGGTCAAC GAGGGGAATC CACTCTGCCA TGGGGAAGTC GCTGCCCCGT 540 AGGGTATAAG AACTTCCCCA TAGTTCACCC CTTCCTCCCT GGCCGCCCAG TCTGGAAGGG 600 GAGCTGGAGA AGGCGGCGGG GGGTGGGGGG AAGGCGGGGG GGAAGGCGGG GGGGTGGGGC 660 GGGCTTCTCT GGTTTCTTAC CCTCCTGGGG TCAGGTTTCC TCAGCTCCCT CCCTTAAGGA 720 GGGGAAATCG AGGAAGAGGC CCATCTCCAT GGAAACTTTC TGGTAACAAG GCTGTGAAAG 780 AGAAGGGGAC AGGTGTTTCA GGAAGAAGGG AAGGCGCTGA GGATGGGCCT GGAGAGGAAG 840 TGTCCCTGAA AGTGGTTTTG GGGCTGCCCG CGCCAGCGAA AAGCACGTGT CCCATTTCCT 900 GCCGGAATGG CCAGAAAAGG TCTCCTCCCC GGCTCTGCCC CCTCTAGCTG AGTCCTGGAC 960 CTCTAGGGAC TCCCACCTAC ACCCTTCCCA TAAAGCCTGA CCCAGCTGGG ACGCAAAGGC 1020 TAGTGTCCCC CTCCCCGAGT CGGTAGGGGC TGGGGAGGGA GGTGGTATGG CCCGGAGCCC 1080 CAGGCCGAGG GCCCGGGCAC CCGTGCATCC CCCCTTCTGC TCCCCATTCT 1130
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