Tag | Content |
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EnhancerAtlas ID | HS091-28542 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:200713690-200715460 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr2:200714980-200714996 | TTCTATGTAAACAAAA | + | 6.15 | FOXP2 | MA0593.1 | chr2:200714984-200714995 | ATGTAAACAAA | + | 6.14 | Lhx3 | MA0135.1 | chr2:200714370-200714383 | AAATTAATTATAC | + | 6.19 | MEF2A | MA0052.3 | chr2:200714562-200714574 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr2:200714562-200714574 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr2:200714560-200714575 | TAACTAAAAATAGAT | + | 6.54 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59686 | chr2:200607740-200722053 | Ly4 |
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Enhancer Sequence | TTCTGGAATA GGAGAAAAAT TTTTATGTGT CTCTAGAGTT GATTCATATT TTCATGTTTT 60 AACTATAAAA AAATCATAAC TTTTTGGAAA CGAAGCAGTC ATAATATGAG CACTTTACTA 120 TTTCATTCCT AGAAAAATTC TAAAGCATAA AATCTCCAGA TTGACTAAAA TAAGAAACCA 180 TGTGTACATG GTCACATACA TATAAACCTT GTAACGACAC TGGAAAATAC CTGGCAGGGT 240 CCTCAGCGTG AATTTCATCA TGTAAGTGAA AGTTTTTCAT TAAAGTATGT TATCCCATTT 300 TAAGCATAGT TTTCCTTAGC CTTATCCCTG TTTTCAAGGT CTGTACTATT TTACAAACAG 360 GTATGTTTTT TTTGTTGTTA AACTAGACTT AGTGGGGAAA TGCAGAAAAA GAAAATGAGG 420 AAGATTATTT AATATGTGGA TTCTTATAAA AGAAATTCTT GCAGCAAAAA TGAAAGTGTC 480 TACAGGCCAT GCCATGGACA TTATACAAAT AAATAAGGAA GCCATTTGGA TGGTTTACAT 540 GACAATTGTC TAAGTTCCTC CTTGTTCCAC CAAAGTTTCT AAATCAGTTT AAAGTCTTTT 600 TACAAAATTC TGTAACTTGA AAGATGATAC ATATTCTGAT ACATATTATT CAATAATATC 660 AAAAATGTGA TTTTTGTTGA AAATTAATTA TACAGGTTTT GGAGGTTGCT TTGATACTTT 720 TTAGTACTCT AGAATAGCAT TTTTGACACA TCTTTCCATA CTTCAAATGA TATTCATGAT 780 CTAAAGGAAT TAAAACATCT TAAAATAATA AGAAAATAAT TTCCCTCTTC AAGTTCAGGA 840 CCTCATAACT TTGGTCTCTT TTAAATACCA TAACTAAAAA TAGATGAGGC CCTCATGAAT 900 TCATTCAACA AATATTTAAT GAGGGTCTTT TTCTGACAGG TAATGTTCCC TGTGTGAGGG 960 ATACCAACCA CTGTTCCCTG TGTGAGGGAT ACCAACCACA GTGGTCTAAC TCTGAGACAC 1020 GCGTTAAACT TTAGAGTTTA AGCTAAAAGT GCTCTGGTGC AAATAATGGT GCTCTCCCTC 1080 AATAAATCCA CTGGCTTGTT CGCCAGGATC ATTCGTTGGC CTAATCATCT TAACCTAGAG 1140 AGAGCTCAGG CTTCGTAGCT AGCTCAGGTT TGCAGGCAGG TTTTCATATC ATGTCCATCA 1200 TCTCATCACT GAAAATTCAT AAAAATTCTG TCATTAGGTT TTTCTAGATA TTAATAACAT 1260 TGTTGTAATA AAGCAACCCA GACCTCTCGT TTCTATGTAA ACAAAAAATT GCTTTACACA 1320 AGGGGTGTGG GCGTCTTCTG GTTTTCATTT GTTTTCAGTG TGTTTATGCA GCTTAATTGT 1380 CTCATCAGGC ACTTTCCCAA CATAATTATG CTTTTTAACA AATGGTGTTT ATGGCAACCC 1440 CTAACAGTGC AAAAGAAAGG ATTAGTTTCA TCCTCTCATT CCACATTTTG ATTCCCTGTG 1500 GACAGCTAAA TCACACAAAG ATGGTGTTAG AAAAATTCAC CTTCACAGCG AAGCTGAAAT 1560 GAGCGGCAGT ACCAGGCTCA GAAAGTGACC CAAACGCAAG CCCCCCAAAA CACTCTGTGT 1620 TTGGGACAGG GAGATCCTAG TCCTCCCAGC TCATCCTTCA ATTACCATTG GATGACCTCT 1680 GGTGATAGAT TAAACACTCG GCCGTCCCCC GCCCCCGCGC CTCCCCACCC GCGGAGAACC 1740 TAGCCTAGCA AGTGCAAAGT GCAGCAGTTC 1770
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