Tag | Content |
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EnhancerAtlas ID | HS091-14308 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:107210640-107212920 |
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) |
RARA(var.2) | MA0730.1 | chr14:107212785-107212802 | AGTTCAGCCCAAGGTCA | + | 6.33 | SNAI2 | MA0745.2 | chr14:107210812-107210822 | TGCACCTGTT | - | 6.02 | Stat4 | MA0518.1 | chr14:107211099-107211113 | CCCTTTCCCGGAAG | - | 6.95 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_58514 | chr14:107149891-107212222 | Ly1 |
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Enhancer Sequence | AACAGTTTTA AAAAATAACA CTACATAAAA GGTTTAAAAT TATTAAAACT TAAATACCAA 60 TGATAATAAA TACATACTAA TAACTGTATG AAAATGTAGC AACCTGTAAG ACTCCAGAGT 120 TCTGAAAACA CAAACCTGAC TTCTCCAGCT GAGGAGAAAG AAAACCTACC GCTGCACCTG 180 TTCCTGGGAC CTGTCCCGCC CTCAGTGAGT CCCGAGCGCC CCCTGGTAGC CCCGCGCGCC 240 CCTGCAGGGA GGTTTGTGTC CGGGCTCACA CTGACCTCCC CTCACTGTGT GTCTAGTACA 300 GTAATACACG GCCGTGTCCT CGGTTTTCAG GCTGTTCATT TGCAGATACG CCGTGTTCTT 360 TGAATCATCT CTGGAGATGG TGAACCTGCC TTTCACCGAC GCAGCATATG CTGTCGCGTA 420 ACTGTTAGCT TTGCTTCTAA TACGGCCAAC CCACTCCAGC CCTTTCCCGG AAGCCTGGCG 480 GACCCAGTGC ATAGCAGAGC CACTGAAGGT GAACCCAGAG GCTGCACAGG AGAGTTTCAG 540 GGACCCCCCA GGCTGGACCA AGCCTCCCCC GGACTCCACC AGCTGCACCT CACACTGGAC 600 ACCTGCAAAC ACAGAGACAC CCTGGTCAGA AAGTGCCACA CACGTCCACT GTTTCTCTCA 660 CTCATGTCCA CTCACACTCA GTATCTCTAG TTCCCCATGA ATCACCTTTT AAAATAGCAA 720 CAAGGAAAAC CCAGCTCAGC CCAAACTCCA TGGTGAGTCT CCTGTATTCA GTGCCGATCA 780 CCGAGTGGAG ACAGCTGGGA ATCCCAAGGC TGGAGCTCCT CTCCCAGAGC TGCAGGGTCA 840 GGGCTGGGCT GCTTTTCATC AGCAAAAAGG GGGGTCTTAT TTGCATGTCT TCTGCTACAT 900 AGCAAGGTCT GGGCTGGGAC GCCTGACGAG AAGGCTGTGC ACAGAGTAGA TGAGGGTGTC 960 CTGGGGGGTG ATTGGTAGTA ATCCTATCAT TCAGGAAAAT TTAATTTCAT ATTATGTGAT 1020 TGTGTCTTGA TATTCATTTA GGAGTAATCA TCTTATTGCA TTTTTTACAT ATTTGCACAC 1080 TGTATTTCCC CTTATATTTT CTGAAGTCCC TTGGCTTGTC TGTTTGAGTG ATGTCTCTTT 1140 CCTCGACACT GTGAAGGGTA TGATGTCATC GTTCACAGGT GCAGTCCTGG ATGTACACGC 1200 AGTTTCCACG GAAATGCTGT CATTTGGCAG TGTTGCCTTC GACAGCCTAA TTACCTGATT 1260 GTTCTACTTG ACCATTTGTG TCTCTTAACA AACCATGTAG ATGTTACACT GTGCTCATTT 1320 CTGACATGTG ACACTGTTTT GTAGCATAAA TCGTTCAACA ATCTGGTGCA ATTAAATTTG 1380 GGCTTCTTTC CGGGGACCAT TTTTGAGGAT TGTTCTGACC CCAAAATAGC ACTGATTTTT 1440 TTCAAGAAAT TAAGTCTAGC TATGTTTCCA GGCTGCGCTT GAAATCCTGG GCTCAAGTGA 1500 TCCTCTCACC TCAAACTCCC AAGTAAATTC AACTGCAGGC AGAGCCACAG TGCCCAGCTG 1560 GTTATTCTTA AATTATAGGT TTTCTAATTC TCTCTGTTAA AATGAGTGGA CTATTGATTT 1620 CTATATTGCT GTCATGGAGC TGTCAGGTTT CTATTAATTA CTTACCATGA AAACCACTAA 1680 CATTTTAGAT GAACTTTAGG GTTGAAACTA TTCTCATTCT ACTGCAAATC TGGTCACGCC 1740 CTTTAGAGAG AGCTTTCTAT CACTGTTTTT ATGCCCTGAC TGTATCACTA GAAAAACATG 1800 GAAGTCTCTA CCTTGGTGCA GAAGAAAGGG TTCAAGCAGC TCAGAAGGAC ACTCCTGCTT 1860 TAAGTACAGA AAACTGCATG GAAGTGATGG ACTTGTATGA TCTCACTGTT CCTCTCCCAG 1920 GAAGCTCCCA GAACCTCTGC CCTACAAGTG AGCTGGGGTG AGAATAATCG GGGTCCACCT 1980 GTTCTTGGTC TATAACACCT GACATGGAAA CTATGTCTTG TGAGTGAGGC TGGGAGGAGA 2040 AAGGCATCCA TCAAATCACA GGCAGGAATT TAGTCTCCAC CATAAAGATC TGACATCATG 2100 ACCTCAACTG AGATCTGGGG GAGAGGGAAG CACCACCTTC TTGTCAGTTC AGCCCAAGGT 2160 CAAGATTCTG TGATCCTGAG ATGTAAAGAA GAGGTAATGC TCTTCTCTCA AGTATTGTGA 2220 TCCTCACTGC ACTTGCTAAG ACTGTTTGAG TTGCTATAAG AGGATATCAT GGACTGGGTG 2280
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