Tag | Content |
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EnhancerAtlas ID | HS091-24287 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:45492020-45493650 |
Target genes | Number: 28 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr19:45492643-45492653 | ACTTGGCACC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 45492316 | 45492894 | chr19 | 45492945 | 45493282 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I044989 | chr19 | 45492541 | 45492710 |
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Enhancer Sequence | CTCATCTTCT AGGCCCTGCA GGCCACTTCT TCCTTGCCCA GAGCACCCCA GTCTGAAGGA 60 GTGGCCTGCG GCCCTGTAGC TCCCGCAGGC GGCAAGAGGA ATGAGTAGTA GTATTCCTGG 120 TATTAAGATG CTATTGCCGG CCTGGTGGTG GCTCTCGCCT GTAATCCCAG CACTTTGGGA 180 GGCCAAGGTG GGAGGATCAC CTAAGCCCCG GAGTTTGAGA CCAGCCTGGG CAACAAAGCG 240 AGATTCGTTT CTACACAATT TTTTTTAAGA ATTAGCTGGG CATGGCAGCG TGTGCCTATG 300 GTCTCAGCTA CTCGGGAGGC TTGGGCCTGA AAGGTCAAGG CTGCCGTGAG CCATGATCAC 360 ACCACTGAAC TCCATCCTAG GCAACAGAGT GACACCCTGT TCCAAAAAAA AGGACGCTCT 420 TGCCATTATT GAGAACTACC ATCTGGAAGA ATGCAGTGTC ATACGGGCAC AGGAGCTGGT 480 GCCGACCCCA GCCAGCCATC TACCAGCTGT CGCTGGGAGA CGGGACCCTT CTGCCTAGGA 540 GCTGGCTTGG CTGGGGTCCA GTGAGAAATG AGGCACAAGA AGGCTGTCCT CCCCAGTGTC 600 ATGCAGCAGG GGGCGCAGGC CTCACTTGGC ACCAGTGCTG TGTGGCCTCC CTGGTCTAAG 660 GAGAGGCTTG GGCCCAACTG CTCCCACGAG AACCCACCAG AACCCTGTCT CCAGACCCAT 720 TCTTCTCAGT TGGGACAGGG GTCATTCTGA TGGGCAGGGG TGGGTGGGGT GAGGCTATGG 780 AGTGTGCCAG AGCTCTGGGA TGTGGGGGAG CTCTGGGATG TGGGGGAGCT CTGGGATGGG 840 GTAGGGTGCA CATGGACCAG AATTCACAGC CCTCACTCCC TGAGTGCAGA GCTGGCCCTG 900 ACTCTGCAGG ACTGCAGACC TGGCTCCACC ACTGTGCTAC AGACGTGGTG GCTCAGCCTC 960 CTGTGGCTGC GGTTAGATGC TCAGCCGGGC GGGGTCAAGA GAGGGGTGTC CGTGGTGAGA 1020 CCAGGGCTCA GAGAGGAGCA TGCTGACATG GATCCTTGGC AGCATCTAGG CGGAGCACTG 1080 GAAGGAGCTC CAGACTGGAG CCCAGGGCCC TTTTCAGTTT CCTGAGCATG GCTGTGAGCC 1140 AGTTCCTTCC CGGTGTCAGG GCAGGGGCCT GGAGGAGGTG GTCTTGAAGT GCATGCCACA 1200 GATCTTCCTT CCCAGGGAGG GCGAGCTGGC ACCATGGTGT GGCACAGACC CCGCGTCCCT 1260 TCAGATTCTG CCATGCCAGG CTGTTTGGCC TCAGGGAAGC AGCTTCCCTG ACCAGTCCTT 1320 AGCACCTGGC ACGTGGTGAG CCCTGTCCAT GGCACCAGTC ACCGTCACCA TCAGTCAAGG 1380 GACTGCACCT TGGGGTGCTG GGTGCTGACG TCCTATGGGA GGGCTCCAGG GGTGCCGCCT 1440 GTCTGGTGCT CTGGGGGTCA CCCAATGAAT ATGAGAGCCT TCCTGGGAGA GAGGGGTCTC 1500 GTTCAGCACC CCTCCTGAGG ACCCAGCCCC ACCCCAGGGT GTGAGGATGC AGGCCAAGGG 1560 GGCCTGAGGG AGCTGCAGTA GGGTCTCAGC ACCTCCTCAG CCTCCTGGTT CCCCCCTACC 1620 CCCTGCGCAC 1630
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