Tag | Content |
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EnhancerAtlas ID | HS111-01778 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr16:1795050-1797020 |
Target genes | Number: 22 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr16:1796280-1796292 | GAATGTTTGTTT | + | 7.22 |
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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 |
GH16I001744 | chr16 | 1794853 | 1797620 |
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Enhancer Sequence | TTGGAGGTCA CTGCTACACG TTGATGTTTA GGAGGTTGAG AGGTTTGCCT TTAGGTAAGT 60 TGTGGCCAGG GGGAGTGTCC CATGGGTAAG TGGTGGCCCT GTAGGGTGAC GGAGAGCTAG 120 GGGAGGCGCA ATCAGACTGC AGAATTCCCC GCAGCCACCA TGAGGGTCAG GAGCAGGCCG 180 GGGACCCAGC GTGGAGGAAG GTGGCCCAGA AGCGTTTGTC TGATGTGCAC AGCTACACCC 240 TGCCTGGCCA CATGGGGTTC CCTGTTTTCT CTCTGCCGGG TGGTGGCAGA GTCGGTGAGA 300 CACCAGGTGC CTGTGACACA TTGGGTAGAC AGGTTCTTTG AGAACGTCAG CACAGACTTC 360 TTGCATGAGC GGTACTCGCT TCCTCCAGCG TGGGGAGTGA CATGAAGAGC AAGGGTTTTC 420 CTTTCAAACT GGGCATAGCT GCAGAGCCAC AGGCCGTCTC AGACATTTCT ACAAAGCCAC 480 TCCGGGAGGC GGGCTGCGCC CGTGTGAGGG CTCTCCCTCG GCACTGCTCA TCTTTTGGGG 540 CTGGACATGC ATGGCCTGGG CCGCTGGGAC GCGGTGGGTG TGGAGCAGCA TCCCTGGCTT 600 CCACCCACGA AAGCCAGGAG CACCCCCTTC ATTTGTGACC ACAAAAATGT CTCTGGACTT 660 TGCAAGCATC CCCTCGGGGC AGTCAGCCCA ACTGAGAATA GCTACTATAG AGGAAGGTGT 720 GTCATTTTGA GATTCCTTCT AGAGAAACTT AGGAGCCTGG TAGATGAAGC AGAAATGTGT 780 CCTCTGAGTG AGTGGCCGTG TCCGGTACTG AGAGGCCCCG TGCCCTGAGT CTGGCGGTGA 840 CCAGAGAGGC TGGGCAGAGG CAGAGGTCAG CACTGGCCAT GACTTCTGGA AGTCCCGTCT 900 GCCCTGGTCA CTTAAAGGCC AGTATAAGTC AGCTGTGGAG AGGGCTGGAT ACCCCCTCGA 960 CAGCTCCTCC CTGGGTGAGA TCCTTAGCAT TAGAGTCCCC CACGGTGCGC CCTCTGAGAG 1020 ACCACGGGAA CCCACCCAGC GGCTGCCTGG GACAGGCACA GGAGCCACCT GGGTGCCTCT 1080 GAGGCCTTGC ACTTTCCCAC ACCTCAAGGA GGGCCGGGGG CCACGGGCAA GCTCTGCCAT 1140 AGCGGGTGAT CAGGTCAGCT AAGACGAGAA CGTTTGGGGC TCTTTTTCTC CAGCTGGTTC 1200 AGTATCTTTG TTAGGAAAGA CCATTGGAAA GAATGTTTGT TTCGCATTCC GCATTAGTCA 1260 CATAGAATGC GCTCCTCCCT AGCGAGCTTC CTGAGGTAGA CGGCTGGTTG CGGTTTCTCG 1320 TAATCCGGGC TGCCCCCACC CTCCAGAATG TCTTGGTGGC GTCCCTTTCT GTGAGCAGGG 1380 ATTGTGGTTT CTTTGCGCTT GCTCATGTTC AGGGGTGAGC TCTGGTCCAG TCAAGCCACA 1440 GGGTCAGCAC CTTCTGGTCA CTCCCTGGCC CTGACCTGAG CCCGGGGAGG AACGTGGGGC 1500 AGGCGCGGGT GGGCCCAGCC TCGAGCTCTT CAGCACAGTG ATGGTGACGG GGCAGCGGTG 1560 GCGGCACAGC CAGCCCTTCT TGGGTCCCCA GTCAGAGCCC TCTGCCCTAC CTGGGCTGGA 1620 CTTGTTTCTG AACAGCCACA AGCTACAGGG GGCTGCCGCT GTGTCCCTGG CGAGGCACTG 1680 GCCCATTACA AGCAATCGTC TGGGGAGGGC ACCAGTGGAA AGCCCCGTTC CAAGCCATTT 1740 CAGGAGGGTG GCCCTGCTTC CGAGGAGCCG GAGTCAGTGG CCGGATAAGC AGAGCCACTC 1800 GGGAGTGGTG AGGCCCGGAA GGGTTAGCCC GGTGGGCGGC AGAGGAGCTC TGGCCCGCAG 1860 GGTGTCGGGC GAGGCAAAGT GCAAAGCATT GGTGCGCGGG GCCTCAGGCA GCCACGGCGG 1920 AGCCGCAGGC CAGGGACCTG CAGTGACTCG CTCTCCCTCC TCCCTGTGTT 1970
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