Tag | Content |
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EnhancerAtlas ID | HS091-25475 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:27584900-27587210 |
Target genes | Number: 31 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr2:27585207-27585228 | CAACAAAAAGAGAAAGTAAAT | - | 6.9 | MEF2A | MA0052.3 | chr2:27586299-27586311 | TTTATTTTTAGA | - | 6.07 | Nr2f6(var.2) | MA0728.1 | chr2:27586510-27586525 | TGAACTCTTGACCTG | - | 6.63 | Nr2f6(var.2) | MA0728.1 | chr2:27585472-27585487 | GAGGTCAAGAGTTCA | + | 7.64 | RARA | MA0729.1 | chr2:27585472-27585490 | GAGGTCAAGAGTTCAAGA | + | 6.45 | SPIC | MA0687.1 | chr2:27585211-27585225 | AAAAAGAGAAAGTA | + | 6.13 |
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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 | CTGTGGCTCA CGCCTGTAAT CCCAACACCT TGGGACGCTG AGGCGGGCGG ATCACCTGAG 60 GTCGGGAGTT CAAGACCAGC CTGACCAACA TGGAGAAACC CCCATCTCTA CTAAAAATAC 120 AAAATTAGCT GGGTATGGTG GCACATGCCC ATAATCCCAG CTACTCGAGA GGCTGAGGCA 180 GGGGAATCGC TTGAATCCAG GAGGCGGAGG TTGCAGTGAG CCAAGATTGC ACCATTGCAC 240 TCCAGCCTGG GCAACAAGAG CGAAACTCTG TCTCAAAAAA AAAAAAAAAA AAAAGAAAAA 300 AGAAAAACAA CAAAAAGAGA AAGTAAATGT GGCAAATTTG ATAACTGTTG CATCTGGTCA 360 TGGAGATTCT TTGTATAGTT CTACTTTTAC GCTGCTTAAA AATGTTTGAT AAAACCAACA 420 TGGCATATGT ATACCTATGT AACAAACCTG CACATTGCGC ACATGTACTG TAGAACTTAA 480 AGTATAAAAA AAAAATTTGA TAAAATGGTT GGGTGCAGTG GCTCACGCCT GTAATCCCAG 540 CACTTTGGGA GGCCAAGGCA GGTGGATTGC TTGAGGTCAA GAGTTCAAGA CCAGCCTGAC 600 CCACATGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAT TAGCTAAGTG TGGTGGCAGG 660 CACCTGTGAT CCCAGCTACT TGGGAGGCTG AGGCAGGAGA ATTGCTTGAA CCCAGAAGGC 720 AGAGGTTGCA GTGAGCCGAG ATAGTGCCAT TGCACTCCAG CCTGGGAGAC GAGTGACTCT 780 TTCTCAAAAA AAAAAAAATT CAATAACACA CATATATACC CAATAGATAA CTCTTCATTT 840 TAAGCTAACC AGTGGTTGGA CTCACAGTCT GGCCCCAACT TACCTTTGCA GTTTGATCAC 900 TCAACAATAA GACTCAGTTC TAGCCTCACT ATACTATGTG ACACTTTTAC ATTGGCCACT 960 CACTTTAAGG CCTATTCTTT GTGTTCAAGC TGTTTCTTCT TTTTTTTTCT TCCCTAACTG 1020 GGCAATTACT TATCTTTCAA GGACTAGGTT AGATGTGACT TGTAAGTTTT CACCAATCTT 1080 TTGTTCATAC TACTACTGGG TTACCTCATA CTGTAGATAC TATCTTCTTA TGCCATGGTA 1140 AGCGTTCCTT AAGGGAATAT AGCACAAAAG TTAAGGGCAC AGTTTCTAGA TCCAGACTGC 1200 CTGAGGTCAC ATCCTGGTTT AGCTACTGAC TAGCTGTGTT ACCTAGGGCA AGTAACTTCA 1260 TCTCTCTGTC TGCCTTGGGT AAGTAACTTA ACCTTTCTGT GTCTGAGCTG TGTTGCCTTG 1320 GGCAAGCAAC TTAACCTTTC TATGCTTCCA TTATCTCATC TGTAAAATCG CATTTACTTC 1380 ATAGAGTTGT ATTATTATTT TTATTTTTAG AGATGGAGCC TCGCTTTGTT GCCCAGGCTG 1440 GAGTGCAATG GTGCCATCTC AGCTCACTGC AATCTCCATC TCCTGGGTTC AAGCGATTCT 1500 TCTGCCTCAG CCTCTGGAGT AGCTGGGATT ACAGGCATGC GCCACCACGC CCAGCTAATT 1560 TTTGTATTTA GTGTAGAGAC AGGGTTTCAT CATGTTGGCC AGGCTGGTCT TGAACTCTTG 1620 ACCTGAGGTG ATCTGCCTGC CTCGGCCTCC CAAATGAGCC ACTGCGCCCA GCCTTCATAG 1680 AGTTGTATTA ATCTTCCTAA ATGGGTAAGA AAGGGTTCAG AACAGTTTCT GACACACAGT 1740 TAAATATTCA ACAAATGCTA ATTTATAAGG TTAGGACTCT CTTTTTGAGA CAGGGTCTCA 1800 CTCTGTCACC CAGGCTGGAG TGCAGCGGCA CAATCATGGC TTACTGCAGC CTCTACCTCC 1860 TGGACTCAAG CAATCCTCTG GCTTCAGCCT CCTGAGTAGC TGGAACAACA GATGAGCACA 1920 ACCATGCCCA GCTAATTTTT ATTTTTTGTA GAGACCGGAT TGCCATGTTG CCCAGGCTGG 1980 TCTCAAACCT CTGGGCTCAA ACAATCCTCC TGCCTTAGCC TCCCAAAATG CTGAGATTAC 2040 AGGAATGAGT CACTGCACTC AGCCCAGGAC TATTTGTTTT CATATTCCTC CTCACACCCA 2100 GTTTAGTGTC TGGCATGTAG ATGCTCAGTG AATGATTGAT TTGGGTAGTT TTGGTTCTTT 2160 ATACGGGTCT TCAGGTTAGT CCCAATGTAC TGGCATGGAG CTAGTTACTT GAGCAGGTCT 2220 TCACAAAGGT CTGAGTAGCA GGTGATAAAA GGGGTTGTGA AGTCTGGACT CCTAACTTAA 2280 GTGGTGGAGA TGCTAAAAGA GAAACAAAGG 2310
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