Tag | Content |
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EnhancerAtlas ID | HS091-23288 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:11697920-11699780 |
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 | chr19:11699569-11699581 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr19:11699573-11699585 | AAACAAACAAAC | - | 6.32 | ZNF263 | MA0528.1 | chr19:11698424-11698445 | AGGGGAGGGGAGGAGAGGAGA | + | 6.23 | ZNF263 | MA0528.1 | chr19:11698437-11698458 | AGAGGAGAGGAGAGGAGAGGA | + | 6.37 | ZNF263 | MA0528.1 | chr19:11698442-11698463 | AGAGGAGAGGAGAGGAGAGGA | + | 6.37 | ZNF263 | MA0528.1 | chr19:11698447-11698468 | AGAGGAGAGGAGAGGAGAGGA | + | 6.37 | ZNF263 | MA0528.1 | chr19:11698452-11698473 | AGAGGAGAGGAGAGGAGAGGA | + | 6.37 | ZNF263 | MA0528.1 | chr19:11698457-11698478 | AGAGGAGAGGAGAGGAGAGGA | + | 6.37 | ZNF263 | MA0528.1 | chr19:11698462-11698483 | AGAGGAGAGGAGAGGAGAGGA | + | 6.37 | ZNF263 | MA0528.1 | chr19:11698467-11698488 | AGAGGAGAGGAGAGGAGAGGA | + | 6.37 | ZNF263 | MA0528.1 | chr19:11698472-11698493 | AGAGGAGAGGAGAGGAGAGGA | + | 6.37 | ZNF263 | MA0528.1 | chr19:11698429-11698450 | AGGGGAGGAGAGGAGAGGAGA | + | 6.42 | ZNF263 | MA0528.1 | chr19:11698419-11698440 | AGGGGAGGGGAGGGGAGGAGA | + | 6.63 | ZNF263 | MA0528.1 | chr19:11698394-11698415 | AGGGGAGGGGAGGGGAGGGGA | + | 6.91 | ZNF263 | MA0528.1 | chr19:11698399-11698420 | AGGGGAGGGGAGGGGAGGGGA | + | 6.91 | ZNF263 | MA0528.1 | chr19:11698404-11698425 | AGGGGAGGGGAGGGGAGGGGA | + | 6.91 | ZNF263 | MA0528.1 | chr19:11698409-11698430 | AGGGGAGGGGAGGGGAGGGGA | + | 6.91 | ZNF263 | MA0528.1 | chr19:11698414-11698435 | AGGGGAGGGGAGGGGAGGGGA | + | 6.91 | ZNF263 | MA0528.1 | chr19:11698432-11698453 | GGAGGAGAGGAGAGGAGAGGA | + | 7.19 | Zfx | MA0146.2 | chr19:11699331-11699345 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr19 | 11698258 | 11698351 | chr19 | 11698490 | 11698957 | chr19 | 11699084 | 11699294 | chr19 | 11698651 | 11699303 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I011587 | chr19 | 11698384 | 11699014 |
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Enhancer Sequence | ACAATGTATT TGGCTTCAGC AAAAAGGTGG TGGTCCACAC TGTCTCCAAG GAGTAAGACC 60 CTCAGACCAG GAGCCCCAGT GACAGTATGA GAGGAAGAGA GAGGCCCTCA GCTGCTTGGG 120 AGTCCCTGCT GCACTCAGCC CCCCACCACA CTGAAAATCT CCCCATACAC AGTTTCCATG 180 CCAGACCCCC TGAAGAACAG GGCCTATCAA TAAAGCAGTA AGGTCCTCTG TACTTAGACC 240 AAAAACAAAA AAAAACAAAA AAAAAACAAA AAATGAAAAT TACTCTTGCC TGTAATCCCA 300 GCATTTAGGG AGGCTCAGGT GGGAAGATTG CTTGAGCCTA GGAGTTTGAG ACCAACCTGG 360 GCAATATGGT GAGACTTTGT CTCCAATATA GATAGATGAT AGACGGATGG ATAGAAGATA 420 GACAGATTAG ACAGAGAGAG AGAGAGAAAG GAGAGAGAGA GAGAGAGAGA AAAGAGGGGA 480 GGGGAGGGGA GGGGAGGGGA GGGGAGGGGA GGGGAGGAGA GGAGAGGAGA GGAGAGGAGA 540 GGAGAGGAGA GGAGAGGAGA GGAGAGGAGA GGAGAGAGAA ATTAGGCAGA GGAGAGGAGA 600 GAGAAATTAG GCAGATGCCT TGGGCAGTGA AGTCCCTGGG GATGGTCTAC TGTTCCCGCA 660 GCCTGAGCGC CTTTTTCAGA CGTTTTTATC TGTCCACTGC TGCCCCTGCA TGGCCACAGC 720 CTGAACTGCA GCACCGAACG CAGACCCAGT TTCCCTTTTG GAGAAGAAAT TAATGCTCCT 780 TCCAGCCCCC CACTTGCCAC TAGGCCTGTG CAGGGCGTGG ACAGATTCTA CAGTGGATCC 840 AGCCAGAGAC TGCCCCAGAG AAAATTCCAG GGGTGGGATG AGTGAGGTAT GCTGGGACTG 900 GAATGTTTGT AGGATAACAT GATGAGCAGC CGGATTCCCA GGAAATTGCA AACCGTGTCT 960 GCTCTGGTGA GATTCTCAGA GGAGGGGATC TATAGGCAGT TCTGAGTAGG CACTGGGTAA 1020 AAGCCTGGAA AGAGGACCCT GGCTTGGATG GGGCTCTGCC TCACTCGCCA TGAGCTCCTT 1080 GGCGCTATCA GTCAGCACAG TTCAGCTGCA TGGGTGTGAA GGTGTCCTGG TGACTGGCTA 1140 CCCCCATGCC TGCCTCAGTG CACGGGAGGT GGAATTATGG ATTTGGTGGG GCTCGCACAG 1200 GCTAAGGGAC TGATTTTCAG TCTGGAGAAT GGGAGGGCAG GATGAGCTGT GGAGGGTCAG 1260 GCTGGTGGTT TGGAGGGTGG CATGATGTAA ATGTAGCTGT TCACTGTTGT AGTTTGCTGC 1320 CACCAGTTCA GTCTGGCTAG GTTCCAGGTG GGTCAATAAT CTCAAATGGG GCTGGGCTCA 1380 GTGGCTCACA CCTGTAATCC CAGCACTTCG GGAGGCCGAG GCGGGTGGAT CACTTGAGGC 1440 CAGGAGTTCG AGACTAGCCT GCCTAACATG GTGAAACCTC GTCTATACCA AAATATAAAA 1500 AATTAGCCAG GTGTGGTGGC GGGCGCCTGT AAGCCCAGCT ACTCGGGAGA CTGAGGCAGG 1560 AGAATGCTTG AACCCAGGGG GTGGAGGTTG CAGTGAGCCA AGATCGTGCC ACTGCACTCC 1620 AGCCTGGGCG ACAGAGCGAG ATTCCACCAA AACAAACAAA CAAACAAAAT CCCAAATCGG 1680 GAGAGGTGAG GTGGGGTCTG TCATGCCAAG GAGTTGGTTT CTTTCTTTTT TTTTTTTTTT 1740 TTTGAGATGG AGTCTCAGTC TGTCACCCAG GCTGGAGTGC AGTGGCGCTA TCTCGGCTCA 1800 CTGCAAGCTC CGCCTCCCGG GTTCACGCCA TTCTCCTGCC TCAGCCTCCC AAGTAGCTGG 1860
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