Tag | Content |
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EnhancerAtlas ID | HS118-01670 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:213910090-213911410 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:213910653-213910665 | GTTTGTTTGTTT | + | 6.32 | TBX20 | MA0689.1 | chr1:213911349-213911360 | AAGGTGTGAAG | + | 6.32 | TBX21 | MA0690.1 | chr1:213911349-213911359 | AAGGTGTGAA | + | 6.02 |
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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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Enhancer Sequence | ATCCCAGTTT GCCTGGACTA GTTTTAGCAC TGAAAGTCCT GCATTCTAGG CAACTCCTTG 60 GTCCCAGGCA AATGAGGATA GTTCGCCACC CTAAACAGAT AACATACCTT CTTTAATTTG 120 TTTTAGGCCA ATATTAGGGG TGAAAGAGAA ACCTAAAAGG TTTCATCCAG AGGTGGTCAA 180 ACTATTCCCC AAGGAGCTCT TTGAGGGCAC TGAGGTGAAG GAGATGGTGA GAGGATGCCA 240 ACAGGATGGG CTTTTCAGCT CCCTCCCGTG TTCCACCACA GAGCAAACCA GCTCCCGGCT 300 TGCTCATACG TGGTGCATTT GGTGTAATTT GTTGTGTGAA GTGTGGTTTC CATGGCCACA 360 GGTTGATACC TTAACAATTT CATTTTACAT ATAAAAAGCC AAGTTCTGTA AAAAACTTAG 420 GGGCAGAATT CAGCCTCTTG ACATGTAAGT CAGACCTCTT CTACAACACC ATCCAAATGA 480 GTTGAGCATT TCTTGGCCAT CTGTCTCATT CACAGCTCTG GACTTGGTGC TGAGGCAGTG 540 AAGAAAGGTT TTGGGGGGTT GTTGTTTGTT TGTTTCCAGT CACATTGGGG AAGACCTAGG 600 CTAATGCTAG AACATACTCA CCATGACCAT GACAGCTTTA TCTGATTTGA TCAGTTACTA 660 AGGAATCAAA ATGGTGATTT CAGCAACCTG GAAACAGGTA GGTTTACCTT GGAGTTACAT 720 GTTATTTCAA AACAACATGG GGACAAGTGT GAATTCTTGA GGTTGAAAAC AGCTTATGTC 780 AATGACAGGG ACTTTCTAGT CTTTTCAGCA TAAAACACAA GCCAGTGTTT AAACTACCGT 840 AGACAGAGTT CATAAGCACA GAGGGAGGGC AAGGTTATGC AACTGGTGAA AAGTACAAGG 900 CAAGGTTAAT GTGGACAAGC AGAGTGGTGG TTTCAGACTG CATAAGGGAA GGTGGTCCAA 960 TTCACTAATC AACATGGCTC TACTACTGCA GCCAGCCCTG TCCTATAAAC CAATCAAATG 1020 GAGTAGCAAC TTATACCTAC AGGCAAGAAA AAGGTCCAGG GCAGTAACTC ACTTCTCCAC 1080 CTGGCCAGCC AGGCTGATTT CTGTCATTTG ACACCATACA GTCTAGGTTG GCTGATAAAT 1140 AGGTCTCACA TCTTGGAATG CTAATCTCGG AACAGTTTGA TTTGCTTCAG CACCATTGCC 1200 TCATTAACCC CAAACTGAGC CTGGGGTGTT CTAAATAGGG TAGTGAATAT AATGTCTCCA 1260 AGGTGTGAAG CTATTTATCC AAGGTTACTT GGTAGAAGAG TTTGCAATAG GGCCTCACTT 1320
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