Tag | Content |
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EnhancerAtlas ID | HS095-17936 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr2:238864210-238865560 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr2:238865290-238865310 | CCCCCACCCCACCCCCGCCC | + | 6.14 | RREB1 | MA0073.1 | chr2:238865291-238865311 | CCCCACCCCACCCCCGCCCC | + | 7.16 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGTGTACCA AGCCTTTCCC CTCACTATTT TTCTCTGCTT TGCTCTGACC TTGGCTCCTC 60 AAGATGCCCC CCTTGGAGGC TGGCCCTACC CTGCAGTCAG CTCTTCGGGC TTCCTCGAAG 120 GCTGGGCACT GCCCCGCTGC CGGTGCTCAG CCTTCAGGGG GCCCGCCGGG TTCCAGGAAC 180 AGCCAGGACC ACCTGTCTGC GGGACCCGCG GAGCCAGGAC CCCTGCAGGC GGAGCCTCAC 240 CCGCAGCCCA ATGCCCGGGT GTCGCCCCCA CCCAACTCTC CTGCCCCGGG AGGACCCGGC 300 TTCGGGGCTT TGGGGAACCT GCGGCGCCTG GGCCACCCCC TGCGTGGACC CCTGGACCCC 360 AGGCGAGGCC ACCAGCGCCC ACCATCCAAA GGGCGACAGG GAGGCGTCCC CCCAACCCCG 420 GCGGCGATGC CTCCTGAGTC CTAACCACAC GCCGTGGACC CCCGCACCCT CAGTAGCCCC 480 GCGCCGAGTG TAACCGCGCC CCGTGTCCTG GGATCCCGCG GCCCGGGTAA CCAGGTCCCA 540 TGTAACCGCA GCCTGGTGAA GCCGTGCGCC CTGGGCGCGG CTACTTGGCC CTCACGGCAG 600 GGCGGAGATG CGAGGCCCCA GGGTTCGGCC CCGCAGCGCC GCTGAGTCCA AGGACCGAGC 660 TGGGAGTGGG GGCGGAGCCA AGAAGGGGCG CCCCTGCGCC CACAAGCCGC AGCGCCCAGG 720 AATCCCCTGG GCGCCTCCGC GTCCCCCGCG GGCTGTCCCG GCAGGCAGGC AGCCCACCCC 780 AGGGCTCCCC TCGTGGAAGG ACACCCCTGC TGACCCTGGC CCTGGTTCTG GCGGTGTCTC 840 CACTCAGCCC TCGGAGGGAC GCCCACCTCC CGCGGAGCTG GGGGACTGTG GCTTCCTCCT 900 GCGCGGGGAG GTCGGTGGGC GCCGTGGACC CGTCCCGCCC CTGTCTGAGG AGCCGAGTCG 960 GCCACAGAGG GGCAGCAGAC TAGGGAGGGC TGATGGGCCG TGCACTTAGC TCCCTCCGGG 1020 CTGCTGGCCG GGGCCCTTGA ACGGACAGAT GCCAACTGGC AGATGAGGGG GCTGCGTCCA 1080 CCCCCACCCC ACCCCCGCCC CCAGGCCGCT TCCAAAGGTT TCTCCCGGAT TCCCACAGGC 1140 GGCCCGCCAG GCCCTGCTTG GCAGCTTGTT CCCTCGCATC CCACCCCCGT TCCACCCCCC 1200 AAAATCAAAA CGGTTCAGGG TTCTGTGAAG TGAAAAGACC CCTGTTCCCG CCCAGAGCAG 1260 CAGCTGGTGT CTGTGGGTTA GGGGTAGGAT TGCTGTCCCC TCGAAATTCA TATGTTGAAG 1320 CCTTAACCCC CAGTACCTCA GAGTTGCTTC 1350
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