Tag | Content |
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EnhancerAtlas ID | HS091-10808 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:110197100-110199720 |
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) |
IRF1 | MA0050.2 | chr12:110198898-110198919 | CAAGGGAAAATGAAAGCTCAG | - | 6.12 | RARA | MA0729.1 | chr12:110198485-110198503 | CCTTGAACGTCTGACCTC | - | 6.8 | TBX20 | MA0689.1 | chr12:110199346-110199357 | CTTCACACCTT | - | 6.32 | TBX21 | MA0690.1 | chr12:110199347-110199357 | TTCACACCTT | - | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_05918 | chr12:110195112-110199905 | Brain_Hippocampus_Middle | SE_65301 | chr12:110195186-110201910 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I109760 | chr12 | 110197886 | 110199170 |
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Enhancer Sequence | CAGCCTGGCC CTGCCTGGCT CACTCTGCGG TAGGTGCCTG GGGTCCCATA TCACAGGCCC 60 TGTGGTGCAG AGTGTTGCAG TCCAAGCTCC CCGCTGCTCC ATGGTCCCTC TGGCACATCC 120 CCAACCCACT CCGCCTGCCC TGCCCCCTCC TCAGCTTCTG GAAGGCCCGC TCTTGTGTCT 180 CCCTATAGCA ACATTAAATC CCACTCAAAG GGCTGGTTTT AATTGGCTTA ATATACTCGT 240 TAATAACCGC ATCTATTTAA CACACCTGTA AAAGGCCCAT AACATTAACT TAATGGCAGC 300 GGCAGTTCGT CCAGCACTTC CAGCCCAGCC AGCCTTTTAA ATTTCCCGAC AAGTCTTTAA 360 TGGGGGCCGC AGCAGGCAGA GGCAGAGTGG GGGAAGGAGT GGCCCCAGTA CACAGTGGGG 420 AGCACCCTGG CTTCTGCACG TTTGAGCCCA GATGCTGCCT GGCGGCTGCC CCTGCAACCT 480 CTCAAAGGCC TGGGAGCGGG ATTCTTTGGC CTTGGAGCCG CCATCCATGG GACGCTTTCC 540 AAGCACCTTC GGTGGTGGCA GCTGCAATTA TTTAGATGTC AGGGTGGTGA GAAAAAACAG 600 GATCTGCCCT AGAAGGTCTC CAAATCTAGC CCAGGAGAAA AGTAGACCGA CAGCTACAGC 660 ATGGGGGTCC TACGAGGGCA CGTCAGGGGC TGCCTGGCTG AGGGACACCT TGGCTGAGAC 720 CTGAGGGTCA GGAGAGCCAG TGGGCCAGGG GTATGTAGGC AACCCCTCTT ACTGCATTTA 780 CCCAGCACAC AACGCAAGCT CCTACTGTGT ACCATGCACC AGTGGGCACC AGTGCATGGT 840 GGAACGCTGG GTGGAGGCCA TCCCTGCCTC ATGGACAGCA CCCCCACACA CACATTTCAC 900 CACTTTGGAT CAGGTGCTGT GACTCACAGA TGAGGCCCTT TGCATAGGGG CGTGGGGCAG 960 GGGAAACACA TACAGACCCG GAGAGCAGTC TGTTCAGGTG GTCAGCACGG GGAGGCAGTG 1020 CTTCAGTTAG ACCCTAAAGG ACCAGTGAGG CTCCGGTTAT GGAGGAAAGA GGGCACATCA 1080 GTGTGAGAGA ATGGGCCCGA GCCACAGTAC CAACGCTGCC CAGTGACTGA GAGCAGGAGC 1140 CAGGGGGATG GAGGACCTGG GCTCAAATCC TGGCTCACAA ATCCTCTCTT GGCCACCAGT 1200 GGTCTCAAAC TGGCAGCCTG TGGACCACAT CCCGCCCACC TGGTGTGTGG TTGGCCCTGC 1260 TGGGTATTTG AACGCTGCTT AAATGTGAAC ATTCTCTGGT CAGGACACAC CCTCCCTGCC 1320 CACCTCAGTC CCTGCCATCT GTCCTCTCTA GGCATTTGTT TGTGACCCCC GCTTGACACT 1380 CTACTCCTTG AACGTCTGAC CTCTTCTGAA GCACGGGGCT GCCACAAGGA CTGCGGAAGG 1440 GCAAGGCCAT GAGGGTTTGG CACAGTGCCT GGCCTGGAGG GAACAGTCAA CAGAGGGTGG 1500 CGTATGAGAG GAAGCTGGGG ACGCCATGTG TGGTTCCAGG GGCCTGCGGG AAGGAGACCT 1560 GGGCCAGGTG GCCAGGGCCT TGAATGCCAC CCTCAGCAGC TCAGACTCAC GCAAGCAGGA 1620 GCTCAGTGGA GGGGTTACAG AAAGAGGCAG CTGGGAGCTT GGAGGCAGTG GAGGGGGCTC 1680 CGATGAAGTC ATCAACCCCA CAACCATGCC CCCACTGAGG GCAGGCACTG AGCTAAGCCG 1740 GCTCTTAACA CCTCTCACAG AACCTCCCAG GTCAGCAGCA GCATTCACCC ATTTCACACA 1800 AGGGAAAATG AAAGCTCAGA GAGGGACAGT GGTGTGCCTC AGGCCACACA GCCAGTGTGT 1860 GGCAGAGCTG GGACTTGAAC CAGATCTGTG GCTCAGAGTC CACGAATTCC ACCTGCAGCC 1920 CCACCCCCAG ATGCTGTAAG GCTGCCCCCC CAGGCCTCTG TGCTCTTCCC AGGAGCAGAA 1980 GCTGCCTCAC CAAGGTGGGT GGCGAGCCAG AAGGGTCCAC GGGAGTACGA GGAGCTTTGA 2040 TGCAGCTGCC AAGGGCACTA CCCCAGGCTC CAGGCAGGAC CCGAGGAGGA CAGGGAGCTG 2100 TGCGCCCCTC CCCCCATCCT AAATCAATAC TCAGTCACTG GCTGCTGGCA ATTATAGAAA 2160 AGCACAGAGG AGTAAAATCC CCCTGCCATC CCATAACCCG GGCCCTCTTC CCCAGGCAGG 2220 CTGCTGTCAG CATTTGGGGC TTGTTCCTTC ACACCTTGGT TCTATCTCCT TCCAGAGAGA 2280 AGGAGAGAGC CTGCGAGGGT GTAGTAAGTT ACAGGCATGT GGGAGCCGCC TCTTTCCATG 2340 TGTCTCCCTG TCCATATCCC CCACATCTCC AGGCCTCTCG AACCTCATGT TTAGGGCCCA 2400 GCAAGTCCCA TTGCTTCTGA GGGCCCCTGG GTGTGGGTAC TCTGCCTGGA GCTGGCAGTT 2460 GGGCAGCTCC CAGGGCTTCC TTTGGCCCCT TTCCAGCCAG CAGCCTGGGG GGTCGTAGGA 2520 AGACCTGAGT CAGATCTCTC CTCTCGGCTC AGAACCTTCC AAAGCAGAGG AAACCCCCGG 2580 GTCCTGGCAG TGGCCCTGAA GCCTGCCGGT TTGCAGTGCA 2620
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