Tag | Content |
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EnhancerAtlas ID | HS091-23456 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:15752420-15754710 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr19:15752497-15752517 | TGAGAGGGGGTGGGCTGGGG | - | 6.31 | SPIB | MA0081.2 | chr19:15752953-15752965 | CACTTCCCCTTT | - | 6.07 | ZNF263 | MA0528.1 | chr19:15752972-15752993 | CTTCCCTGACCTTTCTCCTCC | - | 6.14 |
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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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Enhancer Sequence | CTGGTGAGTG TGGCAGCAGG ACGGGTCTGG GGTCTCAGGG TGGATGGACT TCCTGAGGGG 60 TAAGAATGAG GCTCAGGTGA GAGGGGGTGG GCTGGGGTCT GGGGTGGCAG AGAAGCAGGG 120 GAGGCGTCTT ACTCATTCCT CTGCTTACTC ATTTCTGTGA GGTGCCAACC CAAGCCCTTC 180 TCACCTCCCT GTTCTCCCAC TCTTGGCCTG TGTTGAATCC TTTTCCTGCC TGTCTTTCCA 240 CATTAATGCA CCTCTGCGGG GCTCTTGGGC AGGGGGTTGG GTGCACAGAA AGGTGAACCC 300 CTGGCGTTCC CACATTCTCC ATTGCTGGAC TCGAGGCCTC CTGTACCCAC TGTTCAGGGT 360 CCTCTCCCTA CCTGGCCTAT TTCCTCTTAT GAGGGTATAG GTGGGCCAGA GGAGAGGTGT 420 GGGCTGTCTC TCACCTCCAC CACATCCGGA GGCACCTTCC TCTTATCTTG TTCCTCCCCA 480 GTAAGATGTC CCAATGGGGT CCTGTTGCCA AACCCACATA AAAGTTGGCC ACTCACTTCC 540 CCTTTCAGAA GCCTTCCCTG ACCTTTCTCC TCCCCCAGAC CTTGCCCTCT GACTTAGACC 600 TGCTCTCCCC TTTGCGGAAC GTGGTCTCAA TCTGCTCATT GCAAATGGCA GGATTGATGG 660 GTGTGTCCAC AGGTGAAGTG GGAGGGTGCA CAGGATGCAC TAGCACAGAG CCTGGTGCAG 720 AAGCTTCTCC CAGGTGGGAG CCACTGTCAT GATGGACAGT TAGAGTCACC TCTGCTCCCC 780 TAGTGACTGC TGAGAAGGGA AGGTCCCCTG TGTGCAGAAC CTTCTCCATG GGAGGAACTG 840 GAACCTGTGT GGCTGGTGGA GGAACCAGCC AGGGCATGAA GGGATGTGGG GACCAGCCTT 900 AGGGACATGT CCTGAGTCCA CACTGCTCCC CACAAACCTC CCCTGTGAGG ACCTCCTCAT 960 ATGCCCACCT CTGGGCTGAA ATGACTCCCA GAACAAGGAA ATTTTTCCTC TCAAGCTAAG 1020 TGGGCCTCTG TGAGTGGACA GTGTGTCTTT TCCTTCTGCC TTGGGATGCG CTCTTGGGAC 1080 TTGGGGGTGG CCCCAAGAGA GATAGAGCAG GAGGAATGTA GACAGATAGA TAGGTAATAG 1140 GATAGATGGA TGGATGGATG CACAGATAGG GTGAATAGAT GGCTGGCTGG CTGGATAAGT 1200 AGGTGGGTAG ATAGACAGAT AGATAGATAG ATAACAGGAT AGATGGATGG ATGGACAGAT 1260 GGATGCATGG ATAAGATGGA TGGATGGATG GATGGATGGA TGGATGGATG GATAATACAT 1320 ACATAAAGTA GTAGATAAGA TGGATACATT AGGTGGATAG ATAGGTAGAG TGGATATGTA 1380 GGATGGATAG ATTAGATGGA TGGATAGATA GCTAGATGAT TGATAGATAA TAGGATAAAT 1440 GGATGAGTGG ATGAATGTAC AGATAAGATG GATGGATGGA TGGATGGATG GGCAGATAGA 1500 TATATAGATA GAAAAGTTAG ATAGGATGAA TAGATTAGAT AGATAAATGA ATAGATAGAT 1560 AGGTAGGTAG ATAGATAATA GGCTAGATGG ATGAATGGAT GCACAGATAG GATAGATGAA 1620 TGGATAGATA GACAGATATA TAAGATAGAA TGGATGGATT AGATAGATGG ATAGATACAT 1680 AGAAACATAG GTAGATAGAT AGATTAGATA GATAGATAGA TAGACAGATA GATACATACA 1740 TACATACATA TATAGATACA TAGATAGGTA GATATGTAGA GATATATATA GGTAAATAGA 1800 TAGATAGATA GATAGATAGA TAGATAGATA GATAGATAGA TAGATAGACA GACAGGCAGA 1860 CAGACAGATA GATAGATAGA AGAGGGAGTT TATTTCGGGA ATTGGCTCAC AGGATTATAG 1920 AAGCTGAGAT GCGTCATGGA CTGCTGTCTG CAGGCTGGAT AAACAGACAC TGGTTGTGTA 1980 ACTGAGTCCA AAGGCCTGAG ACGGTGGAGT TCTGGTGTCC AAGGGCAGGA GAAGATGGAT 2040 GTGCCAGCCC CACAACAGAG CAAATTAGCC TTTCCTCTGC ATTTTTGTGC TACCTGGGCT 2100 CTCAACAGAT TGAATGAGCT CTGCCCACAC TGGGGAGGGT GATTCTTCCT TCCTCAGTTT 2160 ACCAAATTGA ATGCCAGTCT CTTCTGGAAA CACCCTCACA GACGGATGAT CAACTATCTG 2220 GGCATCCTTT AGCCCAGTCA AGTGGACACC TAGAATTAAC CATGACAGGA GGTGACGGCC 2280 CCTGCCTTGC 2290
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