Tag | Content |
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EnhancerAtlas ID | HS091-08027 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:66634250-66636310 |
Target genes | Number: 15 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr11:66634552-66634564 | AAACAAACAAAC | - | 6.32 | MSC | MA0665.1 | chr11:66634533-66634543 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr11:66634533-66634543 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr11:66634533-66634543 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr11:66634533-66634543 | AACAGCTGTT | - | 6.02 | Nkx2-5(var.2) | MA0503.1 | chr11:66634862-66634873 | AACCACTCAAG | + | 6.32 | RREB1 | MA0073.1 | chr11:66634276-66634296 | TGTGGGTGGTTGTGAGGGGG | - | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34512 | chr11:66635924-66637087 | HCT-116 |
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| Number: 2 | ID | Chromosome | Start | End |
GH11I066868 | chr11 | 66635781 | 66636787 | GH11I066865 | chr11 | 66632274 | 66635318 |
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Enhancer Sequence | TTCTTGGGGC CATATGTGCT ATGCTGTGTG GGTGGTTGTG AGGGGGGCAG TGTGCAAGGG 60 AACAGGTGCT GTGAAGGCTG GGCTCCTCGA AATGGTAACC ACAGCTGTGA GAGGGTTGCA 120 CAGTGGGTGC TGGGTCAGGA CCTGTCCTTC TGAGGCCTGT TTTCCTGCTG GACTTGTGCC 180 CAAAACCCCC TAGAGATGCT TGGAGAGTGC AAGCTTCCCC ACCTCTGCAG GGTTTTCCAA 240 GCTCAGCCTT ACTGCTCCTA AGGGCAGTCA CAAGTCCAAG TGGAACAGCT GTTTAAAAAA 300 CAAAACAAAC AAACAAAAAA ACCAGGCTGG GCACAGCAGG TCATGCCTGT AATCCCAGCA 360 CTTTGGGAGG CCAAAGTGGG TGAATCCCAC GAGGCCAGGA GTTCGAGACT AGCCTGGCCA 420 ACATGGTGAA ACCCTGTCTC TACTAAAAAT ACAAAAATTA GCCAGGCCTG GTAGTGTGTG 480 CCTGTAATCC CAGCTACTCA GGAGGCTGAG GCAGGAGAAT CACTTGAACC CGGGAGGCAG 540 AAGTTGCAGT GAGCAAAGAT TGCACCACTG CACTCCAGCC TGGGTGACAG AGCAAGACTA 600 TGTCTTAAAA AAAACCACTC AAGGTTTTAC ATGTATTGCC ACTGAGGCTT GTGGTGAAGG 660 CAGCCTGGAA CCTACACTGG CAGGATTTCC CCGTGTTCTT GCTGCCTGCT GGCCCACTTC 720 GCAGCAGAGA TGACAGCTTC CACTCAGTGC CACAGGCCAG GCTGCACTCC TCCCATGCTT 780 CATCTCCACG ACGGTGTGCT GAGAGCCCTG TCATTCCCAC CAGAGGAGGA GCTCGAGGGT 840 CAGAGAGGTT GGAGCTCACC CAGGCTCCAC GTGGCTTGGG ACCTGAGAGC ACCTGAGCCC 900 CAATCTGTCT GACACAAAAC CCGTGCTCCA CAGCAGACAG ACTCCCATCC CTAACAGGAC 960 GCTCTAAGCA GACCCAAGAC CGAGGAGTTC ACAGCAGCTT GAGGGGAAGA GTCTCACTCG 1020 GCCAAAGTGT TGGCCTTGTC TCTAAGCTTC TCCTAAGGGG AGGGAGGGGC CTCCATGCCC 1080 CCGGCGAGCC ACAGCAGCCA CCCCGACAGC ATCCTCAGTC TCAGGTGGGG TTGGGGCTGG 1140 GGGCAGAACT GGGGTCAGGG ATGCTCCACA GTGAGATGGG CTGGCCCAAA GCAGCGTCAA 1200 GAAATTACAT GGCTCATAGT AGAGACCTTG AAGGGTGAGG GCCATCATGA CTGTCATTTA 1260 GAAACCAGGC GGATTTTGAA AATGTCATCC TCAGTGCCTG CAGGGAGCAC GCTAGTGCCA 1320 CCTCTCTAGA GGGCTGTTCC GAGGGATGCT ACTTATCCTT CAATCAGATA ATCCTGTTGA 1380 AGGGTTTACC CTCAGAACTC TTCAGAGCTG AAGCCAAACA TTCAGGCACA CAGATGATAA 1440 GTGACACGCT TAATAACCAC CAAAGCCAGA CACACAAACT AATTGCCTAA CAATCGAGGA 1500 CTATGTAAGT TAAGAAATAC ACACAAGACG GAATAGTACG CAGCCACTAA AAGTATTCAG 1560 ACAGAATTAT GGCCTGGGGA AATGCCTTCA ACAAATATTA AATAATTTGA AAAGTAGAAT 1620 AAAAATTCTA TATAAAACAT CTCTATTGCA TCAAACTATG TCTCTAGTAA AACAGGTAAA 1680 CCGGGAAAGG AGCAAACCAA AGACAGCCGG AGATGCCTGG GTTCCAGCGC CAGCTGTGTG 1740 ACCCCGAGCA ACTCTCCAAA TGTCTCTGAG CCTTGCTTTA CTCCTCTGAC AGATGGGAGC 1800 ACCTGGGCCT GAGCAATCGG CAGCGTCCTG ACAGAGAGGA GGGCTGTCAG TCATTTTTAT 1860 TTGCTCCTTT GTGCTGATTT TTATAATAAC CACGTAATGC TTTTAGAATA ATGACTTTTA 1920 AAACACTAAG TACCTGGATC CCCATTGCTC TCCACCAATG TGGGGAGTGA GCAAGCCCCC 1980 TGGCTGGCCC CAGGAGCCAC TTCGCCTGTA CTTTATGCAA ATCCTAGAAG CCGCGCCTCC 2040 CGCCCCGCCT GCCCGCCCAC 2060
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