Tag | Content |
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EnhancerAtlas ID | HS091-14091 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:100610570-100612750 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2C | MA0524.2 | chr14:100611012-100611024 | TGCCCTGAGGCA | - | 6.18 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_17314 | chr14:100612171-100614800 | CD4p_CD25-_CD45RAp_Naive | SE_23614 | chr14:100610526-100615265 | Colon_Crypt_1 | SE_23822 | chr14:100610367-100618738 | Colon_Crypt_2 | SE_24776 | chr14:100606794-100618712 | Colon_Crypt_3 | SE_31785 | chr14:100606840-100615721 | Gastric | SE_52768 | chr14:100610298-100615730 | Small_Intestine |
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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 |
GH14I100140 | chr14 | 100606368 | 100615136 |
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Enhancer Sequence | GCACCCTCGG GCTCAGGCCC TCGCATTGGT CCATCACGCT CCGGGCTGGG GATGCCCCTT 60 TTCAGAGAAG GGCCCGGGAC CACGGTGACC AGGAGTCGTA GGAGCAAGAT GGCGGTCTTC 120 GACAGGAAGC TGGGCTCAGA ACATTCCCAA GCCCCGGGAA GGTGGGGTGG TGTCCTGGGG 180 CTGGGCCTCA GGTCCTGCCT GTAGGGAACT CCCTACGGGA TCTCCAGGAA GATGGTCCCT 240 CAAGTGCAAC CCACACCCCC GAACCTCAGA GGACTCCACG TGCATTCTGA CGGGCAGGGC 300 CCTGCGAGCG TCCTGTTCAG GGGAGGGATG GACTTGGGGC TTAGCAGGCA CCAGGCAAAT 360 GCAAGGCAGC TTTGCCTTCT CCTCGGCCCC ACAAAGTCTC CTGGGAGGAC CACCTGGCCT 420 GCAATGGGCT GTCCCAGGCC CCTGCCCTGA GGCAGCAGCC AGAGACAGAG GTTCTGACCC 480 TCAGCTTCAA GGAACCAGGG CCACCAACAG GCAGGCCTTG AGATCCTGTG ACCACTCATG 540 CCCCCAGTTC TCCCACATGA CCTCCTGCAG CCACAGAGCA GTGTGCCCAG CAGCCCCCAA 600 GGGCCATGGC AGGGGAGGGA GCCGGCACTG CCTGCTGGGA CCCAGTGGCT GATCTCAAGG 660 GCCGGCTCCT AGCACACTGC ACGTTGTTGG GCTTCCCGGC AGCCCTAGCA ACAGGAATAT 720 GACTGCTCTG CCCCTTAGGA GGCTCCACTC TCTGAGTGGC TTCGCCTAGG CTTCACCTAG 780 GTCTGGTGGC ACTTTTAACC CAGGGCCTGC AGACCACAGC TCAGAGCTGC TCTCTCCCGC 840 TTCCCTGCCG CCCCCCAGGC CAGGAGGGCT CCCCCCAAGG CCAGGAGTCT CCCCAGGAGC 900 GCTCAAAGGA CTGTCTGTCT TCGGAGCCAC CCTCTGACCC TGGGCCTGGC CTTCAGTTTG 960 TGGGTGAGGC CTGGACATGC CCCTTTGCGC TGTCTGCAGA AAAGTGTGCT GAACGAGGCA 1020 CCCCCTCAGG CACAGCAGGA GGAGCGGGTG CTCTGGGTTC CCCTCAGCCT GTGGGCGGGC 1080 CTGTGTGCAC AGGGAGGGGC CGCCCGGCTC AAAGTCCTGG TGCCGGGGCC AGCAGCACTT 1140 CCTTTGCAGA ACAAGTCCTG GGCTCAGGCC TCTTCCCTGC GCCACTCAGC AGGCTGCCCA 1200 CTCGGACATG GGAGGCCGGC GCTGTGCGGG GCCACTCCCA GGTATAGGGG GAGACCTGCA 1260 TCTCCCAGGT CAGCAGGGAC AGCCCCTGGC ACCCCACTCA TGGAGAGGCC TTCAAGCCCT 1320 GACTGTAGCC TCAGTCTCCA TTCCTAAGTC CTGGAGGCTG AGGCCGCCTT CCCCAAGGCA 1380 GTGGTGGGAG CTGCATCCAC TGCTGGATTG CAGTGGGCCC GCTCCATCCC TCTCTGGCAG 1440 GGAGGGCCTC CTCGCTCAGG CACCCCTCCT GCTGCCTGCC CACCTCTGGG ACATCAGGAC 1500 CCAACCCAGC CCTGCCCTCC AGGAGAAGAC AACCTCCTAG GTCGCAGCTG CACCCTCAGC 1560 CCTTCTGTAG AAAGGACCGA CACGTCTCAC GTCACGCACA CTCCCAGGAC GCTGCCCGAC 1620 CCGCATCCCA TCTGAGCTGT GGCTCACCAG GACAGTCACC TGCCCGGCCA GCCCCCGGGC 1680 TTGGGTGCCA GATCTGGGCA GAGCTCCTCC AGCCCCTCCT CCGAGCTGGT GTGGGGGATA 1740 GACCCTCTCT GGGCTCAGGG ACGCTCCCTG CCGCGGGAGG GCATACAGAG AGCAGGAGGT 1800 GAGCAGGCCC AAGGGGTGGG GGCAAGGCAG GTGGTGTGGG CTCAGGGGGA TGGGGGAGCC 1860 AGCCTCTGCG TGGCTCAGCC AGGCAAGGGA GCCGTGGGAT CCCCGGGCTG CTAGGAGGGA 1920 TTTGGAGCCA CACAGATGAC CAAAGTGAGC TTTCTGCTGT CCACACCTCA GTGTGTGTGC 1980 ACACCACAGT GGCAGGCCCT GAGGGAGCAC TGCCAGCAGC AGCCACCGTC CCACAAAGAG 2040 CCAGGAGTGC ATGGCAGGAC CTGGGCCTGG CCTGGACGAA GCGGCACTCA GGCCTCAAGC 2100 TCCACTCATC GGGGCGGCCC AGCGCCCCAT TCCCTGGGGC CAGGCTCAAG CCCAGACCAC 2160 CCCCTCAGAA GCACAATCCA 2180
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