Tag | Content |
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EnhancerAtlas ID | HS091-00596 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:17277620-17279790 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:17278352-17278371 | TCTCCAGGAGGTGGCGGTA | + | 6.24 | Nfe2l2 | MA0150.2 | chr1:17278707-17278722 | TGCTGACTCATGCCT | - | 6.37 | Nr2f6(var.2) | MA0728.1 | chr1:17278602-17278617 | CGAACTTTTGACCTC | - | 6.4 | RARA | MA0729.1 | chr1:17278599-17278617 | TCTCGAACTTTTGACCTC | - | 6.38 | ZNF263 | MA0528.1 | chr1:17277745-17277766 | GGAGGACTGGGGGGATGGGGA | + | 6.17 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_69143 | chr1:17278669-17281247 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 17278702 | 17278792 | chr1 | 17279039 | 17279270 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I016951 | chr1 | 17278181 | 17278930 |
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Enhancer Sequence | CAGGCAGCTG GGGAGGGGTG GGCAGGACTC TGAGCCAGTG TTTCATCATC GTTCTTGCTC 60 TGCCTCGGTC TCTACATCTG TGAAATGGGA CTTCCTCTCT GTTGTGGAGG TCCTGGGGAC 120 AGCTAGGAGG ACTGGGGGGA TGGGGAGGTT GTGGTTCTTA TTAGACATGC AGATTCCCAG 180 GTCCCAAATC TGGTCCAGCC CTGGTAATCC TGATGCAGAG GGTCCACAAC CACATTTGGG 240 AAATACTGAC CTAATGTACA GCAGGAAAGC ACTTTCATTT GCTAAGAAGT ACTGTTTGCA 300 TATGAAGAGC CACTCAGACC TCAGCATATA GAAAGGCAAG GGGCCAGGGA AGTTACTAGA 360 ACACTGACTC TGGGTTTGAA TTGCCTGGGT TTGAATCGAA TCTTGGTCGC TTACTGGTGA 420 TGCTACCCAA GGTGTCCGTG CCTTCATTTC CCCACCTGTA GAAATAGGGA TAGGATAGTG 480 AAAGGTATTG AAGATGAGCT GAGACCATCT GCATAGAGGG CTTAGCATAG TGACTGGTAC 540 TTAGCAAATG CTCCATAAGT TATGATTGCT GGCACTGACA TGCTCTCCAG AGTGGCCCTC 600 GGGACAGGGG CCCTCAGCCA CCAAATCCTA GACAGGGCTG CCTCTGACAG AGGTGCAGGC 660 TATGACTGCA TGGCTCCAGG GCATGCCACT CACCCTGCAG TACCCCTGGC CTTGGGTGGT 720 TGTTACCACG CTTCTCCAGG AGGTGGCGGT AAAGCTCTTT TTTTTTTTTC TTTTTTCTTT 780 TTTTGAGACG GAGTCTTGCT CTGTTGCTTA GGCTGGATTG CAGTGGCGCA ATCTCGGCTC 840 ACTGCAACCT CCACTTTCTG GGTTCAAGCG ATTCTCCTGC CTCTGCTTCC TGAGTAGCTG 900 GGATTATAGG CGCGCCACCA CGCCTGGCTA ATTTTTGCAT TTTTAGTAGA GACGGGATTT 960 CACCATATTG GTCAGGGTGT CTCGAACTTT TGACCTCGTA ATCTGCCCAC CTCGGCCTCC 1020 CAAAGTGCTG GGATTACAGG CATGAGCTAC GGTGAAGATC TTAAAGAAGG GGCGGTTTGG 1080 CCGGTCGTGC TGACTCATGC CTGTAATCCA GCACTTTGGG AGGCCGAGGT GGGCAGATCA 1140 CCAGGTCGGA AGATCGAGAC CATCCTGGCT AACACAGTGA AACCCCATCT CTACTAAAAA 1200 TCACAAAAAA TTAGCTGGGC GTGGTGGCAC GCGCCTGTAG TCCCAGATAC TTGGGAGGGT 1260 AAGGCAGAAG AATCGCTTCA ACCTGGGAGG CAGAGGTTGC AGTGAGCCAA AATCTCGCCA 1320 CTGCACTCCA GCCTGGGTGA CAGAGCAAGA CTCCGTCTAA AAAAAAAAAA AAAGAAGTGG 1380 CAGCTCTGTC TGCTTCTCAC AGAGTTGCTA GGGGCAAGTG CTGAGGCAGG CACCTGCCCT 1440 CAGGCTCCCC AGGTGGGCTG CTATTTGCCT GTGGGCTCTG CCTGCCCGCC TGTCCAGTCC 1500 CCAGGGATCT GAACTCCTGT GACCTCCCCC TTGCTCTTCT TGCCCTTTGC ATTGCCTGGC 1560 TTGGCCTCAT TAATGTCCCC AAATCTGTGT TCTCTCCAGC TCCTCTGGCA ACCCCTGACC 1620 CCCTTCATTC CTCACAGCCA GTCCTAACTC CCCTCCATCC CAACCCCAAT CCCTCTTCCA 1680 CAGCTGTCGG AACATCCCCT AAGCTAAAAA TCAGATTGCT CCTTGTCACC TTGGCTCGAG 1740 TCCTCTCTCC CACTCCCCTC ACTGTCCTTA GAATCCCCAT GGCCCACACG GCCTGTCCTG 1800 GCCCCACCCC TGCCTGGGGC TCTGGCCCTG TGACTCACCA TGTCCCGTTC CCCTCTGCAC 1860 CCTGCATCCT CTAGGCCTTT CCAGGGGCTG TGTTCTTGGC CTGGGGTGGT CTTTTCTCTC 1920 CTTACCTGGC TGACAGTTAC TTGTCCCTCC GCAGGGGACC ATGTTCGGAC CCCCAGGCCA 1980 GCCCACTGCT GCTCCTTGGC ACTTTCACGG CCCTGGCGTG TCCCCGTCAT AGCCCTTATC 2040 ACTCCCTTGT ATTTACCTGG TCACCCTCCA TCTCTGAGGG TATGGGGGCC AGATGGCTCT 2100 TGCTGCCCTG ATGTTTTGGG GGGTCTGCCT GGGCCCCCTC CTGGTGTGTC ACAGGCATCC 2160 GGTCCTGGCC 2170
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