Tag | Content |
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EnhancerAtlas ID | HS170-00656 | Organism | Homo sapiens | Tissue/cell | RS4-11 | Coordinate | chr11:70282690-70284030 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxa2 | MA0047.2 | chr11:70282885-70282897 | TGTTTACTCTGG | + | 6.11 | Nkx2-5(var.2) | MA0503.1 | chr11:70283686-70283697 | CTTGAGTGCCT | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 70283200 | 70283800 | chr11 | 70282839 | 70283157 |
| Enhancer Sequence | TTTGCTTTGG TCTGTGGTCA CTCCGTTCTG CAGTGGAAGC TGCGTCGACA CTCTCGGTGT 60 CCTGCGCCCC GGACCTGGGC TGGCGGAGGC TCTCCTGCCG TCCAGTGCGT CTCACGCGTT 120 CTGTTCTGGC TTTAGACCGA ACCGTACGTT CCCTTTTCAG TGTTCATTCA AAGGTGCTGC 180 TTATGAACTG AAATGTGTTT ACTCTGGCAG ATGATTCAGT TTTTTGCACA AAGGTTCCAA 240 GCAAAATAAA ACACTCTGTG CTTAAAAGTC ATTTCTGAAT TACAGTTCTC AAATCCTGAG 300 GGGGATTTTG CTCCCAGTCT CGTTTTGCTC AGGGGCACCA GAAGTTAAAG GCTAAGGGGA 360 ACAGTGGCAC TGAGGGAGCA GGTGTGCCCT CGGGAGCCGG GGGTGCTGGG GAGCTGGGTT 420 CCGGCTCACA CTTCTGCCCA TCAGGTGCTC CCAGGGAGCT TTCGGCTACA CGACATGCCT 480 GCTACCCCTT CCAACCTGGG TGGTGACGGA GCACTGCCTC CTCCCTTGGG CTGTCCCACA 540 CCTGCCTCTG GCTTAGGAAA CAGTGCCTCT GCCAGCTCTG CCCACAGGAG CCTAACGTGA 600 GAGTGCCCCC GCCCTCCTGC CACAACCGGG CTGCTGTGGG TTCTGCATCA CAGGGTTGCA 660 GCCCTAACGG CGAGCCCCGT CCCACACAGG GCCTGTCTGC TGGGTGAGAT TGCAGCCACC 720 TGCAGGGAGC TGAGTCCTGA AGAAATGAGG CATGAAGGCT TGTGAACCAG GGGAAAGTCC 780 CAGCCAGGGT GGGCAGACGG GGTCAGGGGG CTGGAGGACA GGGTGTGACG AAGGGAGGGG 840 GCCATGCAGA AAGGGCCCCC GCTGGCCCAC TGTCTGCCCA GTCGGTGTGT GCCTGTGCCG 900 CCTGCGGATG AGCATGGCAG GGGCTCAACA GGAGCGGGAC ACATCTTGAG TGGGTCTGTG 960 TTTCTGTTCT ATTGGTGGCC AAGCGTGGCC TGGCAGCTTG AGTGCCTGGA GCCAACCACC 1020 TGAATCTTAG CCGCTTTCTT TTTAGATGTG GTTGGGGTTT TTTGTTTCTG TTTCTTGAGA 1080 AAGGGTCTTG CTCTTTCGCC CAGGCTGGAG TACAGTGGCG TGATCTCCGC TCCTGCAACC 1140 TGTGCACCCA GGGCTCAAGC AATCCTCCCA CCTCAGCCTC CCAAGTAGCT GGGACTACAG 1200 GTGCATGCCA CCACACCTGG CTACTTTTTG TATTTTTAGT AGGGACGTGG TTTCACCATG 1260 TTGCCCAGGC TGGTCTAGAA CTTCTGACCT CAAGTGATCT ACCTGCCTCG GCCCCCCGAA 1320 GTGCTGGGAT TACAGGGATG 1340
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