Tag | Content |
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EnhancerAtlas ID | HS118-11198 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr20:5192250-5193120 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Tcf12 | MA0521.1 | chr20:5192817-5192828 | CAGCAGCTGTT | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 5192510 | 5192995 | chr20 | 5192531 | 5193048 |
| | Number: 1 | ID | Chromosome | Start | End |
GH20I005211 | chr20 | 5192187 | 5193501 |
| Enhancer Sequence | CAGCCTTGAC CTCCTGGGCT CAGGTGATCC TTCCACTCAG CCTCTTGAAT AGCTGGGACT 60 ACAGGCGTGT GCCACCATGC CTGGCTAATT TTTAAGGCTT GTAGAGACAA GCTTTTGCCA 120 TATTGCTTAG GCTGGTTTTG AACTCCTGGC CTCAAGTGAT CCTCCCTCCC CACCCCCTCT 180 CACCTCAGCC TCCCATAGCT ATGGGATTAC AAGCTTGAGC CCCTGCAACT GGCCTCGTTT 240 TACTTTGTAA ATGTGGTTAC TACAAAATTT AAAATTACGT CTGTAATTTA GCTGCATTGG 300 TAGCTTGTAT TATATTTCCT TTGGTTATTG TGTGCTCCAC TCTTACCTCA TACTAGGAAG 360 TTAGGACTTA GGTTATAGCC CCAGCGTCTG ACAGCTGATA AGAAGTGGAA TCAAGGTTCA 420 AGCTGAGTCC AGAGCCCACA CACTGAACTG CTGGACATGC AGGACAGCAT GGCAGTACTT 480 TGGACATGCC CATTGCTTCT GCCACTGGTT TTCACTGAAG AAACCTCCCC CAGTGGCCTC 540 TAGGCTCTGA GAACTTTGAA CCTCATGCAG CAGCTGTTGC AACCTTAGGC ATGGGAAATG 600 ACATCCTTAG ATGCCCTTCC TGATGGGCAG CTGGTGAGTC TTCTTCCAGC TATTTTAGTG 660 AGGTGGGTAG CAGTGCATGG GGTTGCTGAG GCACGCACCC TCGGAACATA TTGGTGTCTC 720 TCCCTAATGG GGCAGCCTAC TCTGTACATG TCAGAAAAGG TGCCTGTGAA GCTGGCAATG 780 TGAGCTTATA TGATCCTGGC CATGTTGGCC ACAGGTAGGA TTAGCCATTG GCAAAAAGCC 840 AGGTTGGCCA AGTTTATTTC TGGTGCCTTC 870
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