Tag | Content |
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EnhancerAtlas ID | HS091-24545 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:49804100-49805820 |
Target genes | Number: 34 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:49804697-49804716 | CAGCGCCCCCTAGTGGCCT | - | 8.17 | SREBF2 | MA0596.1 | chr19:49804446-49804456 | ATCACCCCAT | - | 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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| Number: 1 | ID | Chromosome | Start | End |
GH19I049301 | chr19 | 49804454 | 49804937 |
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Enhancer Sequence | GAGTTCGAGA CCAGCCTGGC CAACGTGGGG AAACCCCGTC TCTACAAAAA ATACAAAAAT 60 TAGCTGGGCA TGGTGGCACG TTCCTGTAAT CCCATCTACT TGGGAGGCTG AGACAGGAGA 120 ATTGCTTGAT TCCGGGAGGC GGAAGTTGCG TGAGCCGAGA TCAGGCCACT GCACTCCAGC 180 CTGGAAGTCA GCGAGACTCC ATCTCAAAAA TAAATAAATA AATAAAATAA AATAAAAATT 240 ACTCTGGAAG AATTGAGAAG TCGGCTTCAG CTGACTTTTA GTGGGAGAAA GAACCCTAGA 300 AAAACCCATA CAGAAAGGGT GGAAAGAACA ATTCCATTTT GCCCACATCA CCCCATCCCC 360 CGAGCCAGCA CTGCTCAGCA TGGAGAGGGA ATTCCCTGGC TCGCATAACC CTCTTTCAGG 420 GATAATGAGA GCAGGCTATA CCACCAGCTT CCCTAGTGTT TTGGGACACT GCCCAACCAG 480 CTTCAGTTTC ACTCCATTCA CATTTCCGTG GGGACTGGCA TTGCCGAGAC TTACGGAGAT 540 AATGGGGAAC CAAGAAGTGG GACAGGCTGT CAGTATCAGC CATGCTGGTG GGAGCCACAG 600 CGCCCCCTAG TGGCCTGCTC AACACGGGTC TCTAGCACAC TTCTGTACTG AGGACCTCAA 660 CAGCACTCCT GGCCACTGTG CAGCTCCCCA CAGTTTTCAC CACCAAGGAC ACCTTGGTGT 720 TACCAATGGC TGATGCCAGC ACCATTTTCT GCAGAGGAAC CAAGCAGCTT TCACAGCTGA 780 GGAAACCAAC TGCCAGCACT GCAGCAGCAA AAGCCCTGTA GTTTTTTCCA CCTTCACAGT 840 CTCCAGGTGC CTGGCCCTCT AATTTCTCCT TCCTCTGTCC CTGAAACCAC CTAAGCTGTT 900 CAATACCATG GTCACCCAGA CCAGACCCAG GGACTCACCC CAGTGGCCAT CGCATTCTCT 960 GGGTGCCTAA GCCAATACCC CTCCTCTATG GAGTCACCCC AGCTGCTGCC TCTACAAGTG 1020 CTCTGAGCCA AGGACCCAGC ACAGCTACCA TGCATGTGCC TGCACACAGC CATGCCTCCC 1080 CATCCCCAGG TTCTAACTCC AGCATCACGT TTGCACCCTC AGCTAGGCCC CGCGGCTGCA 1140 TGTGCACACA CGCCTCCAGC TCAGCCCTGC AACTGCCCAC GTACATGCAG ATGGACTGAC 1200 CTCTGTGGCC AGACTGCAGC AGGCCCCTGC AGTTAGGCAC AAGCTGTCAG GCCCCACTGC 1260 CACATGCATG CCCTTAGTCA ACCCCAGCCC CTGCCTCTGA CTCCACCCCT TGCCACCATT 1320 AATGAGCCTG CAACTAGCCT CTGCTGCCAT GCTTGTGCCT ACAGCCAGCC TCTGCAGCAG 1380 AGTGTGTGCA CACCACTGAC CCCAGCCTCC ACTGCTGCGA GTCCTGGCCC CTAGATGCTA 1440 GGCAAGAGGC ACAGCTGAGG TCCCAGAAAA CTCTGTGGGA GGTTCACAGC CACTGTGGAC 1500 CTCCCACAGC TGTTGCCACC AAGGACCATG CAGGTATCAA CATCACAGCC CCCAGCTGCC 1560 TGTGCTAACA AGACTCTGTG TCCCTCCAAC CTGGACCCAC CACACGCACC CCCACCCACA 1620 GTTGGCACTC TGTGCCACTG GACCCAGTGC CAGAGAGCAC CACTCTTCTC CCCAAAAAAA 1680 GCATTTGAAG TTAATGCTTC TTCAAATGCT TTTCTCAAGA 1720
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