Tag | Content |
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EnhancerAtlas ID | HS091-14200 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:103571410-103573120 |
Target genes | |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr14:103572229-103572248 | CTGTGCCACCTGCTGGCTG | - | 7.01 | CTCF | MA0139.1 | chr14:103571442-103571461 | TGGCCAGCAGGGGGCGCGC | + | 7.76 | NR2C2 | MA0504.1 | chr14:103571502-103571517 | AGGGGGCAGAGGTGA | + | 6.1 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_33976 | chr14:103571486-103572320 | HCC1954 | SE_34594 | chr14:103571115-103572206 | HCT-116 | SE_50540 | chr14:103569707-103572763 | Sigmoid_Colon | SE_57040 | chr14:103569753-103572539 | VACO_400 | SE_59574 | chr14:103557209-103581735 | Ly3 | SE_65696 | chr14:103569523-103572493 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I103103 | chr14 | 103569664 | 103572664 |
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Enhancer Sequence | TAGGGCTCGC CCGCTCCTGT GCGGGCGCAG CGTGGCCAGC AGGGGGCGCG CGAGCGCCGG 60 GAACCTGGAT GGAGGGGAGT GCGCGCGCGT GGAGGGGGCA GAGGTGAGGA GTGTGTGTGT 120 GTGTTTGTGT CTGTGTGTTG GTGGATCTGA GGGGTGTGTG TGCGTGTGTG TGTAGCAGAG 180 TTGGGGGGTG TGTGTGCGTG TGTGATGGAG CTGAGGGTGT GTGCCTGTGT GTGCATGCGT 240 GGAGAGCTGA GGCTGTGTGT GTGCGTGTTT GGCAGAGCTG AGGGCTGTGT GTGTGTGTGT 300 GTGTGTGTGT TGGAGCTAAG AGGTGTTTAT GCATGTGCGT GTAGGGGTGG AGCTGAGTGG 360 TGTGTGTGTG TCAGAGCCTA GATGCGTGTG TCTTGTGTGT GTGTGTCCAT CCGAGCAGGG 420 GCCCTGGGGG AGTGTGGATG GCTCTTCAAG GCTGAGCAGA GGCCGAGGGG TTCCAGCTCC 480 CTGCCTGCTG CCCTGGGCTC CATTTTTCCC TCCCTTCATC CCAGGCAGCA TTTCTTCCAT 540 CTTGGGACAC CTCCTTCTCT GGGAAGCCTC CCTCAGCCTG CACCCTGGGC TTTGCTGGGG 600 TGAGGTCTGG GTCTCTGTGT CCCCAGAAGG CAGACGCCCT CCCTGTGGGC TGGCAGTAGC 660 TGTTGGCCTT CCGTGCCCTC AGCTCCAGGC CAGGCCTCAG CAGATGCGGC AGCGCCAGAG 720 GCACAGACTG AGCCTCCCCA TCTGGGTTTA TCCTTTTTTA AAAGTGTGTA AATTTTAGTG 780 TCCCGAAGTA CTTCTCATTT GTCTGACTTC AAAGAACAGC TGTGCCACCT GCTGGCTGTG 840 TGCTCCGGGA CAAGCCACCT CCCCTCTGTG GCTCTTTTGC CACCTGTCAA ATAGGATCAG 900 AGCACCTGCT CCCTGGGGTG GTGTGGGACC TCTGTGCCTC AGGGGACTCA GTTCCCATTG 960 GCTCTTTGTG AGCACTTCTC AGTGCCAGGC ACTTTGTGGG TGCCTTCCCT GCCTGACACG 1020 TCTCATCCCA AGCGCAGTAT ACCCACGCAC AGGTGCAGAG CACAGGCCTG GAAAGGAGGT 1080 GCCACTTGCC CGTGGCCACG TAGCCAGGAA GTGGTGGAGC TGGGACTTGA ACTAGGCCTG 1140 CCTAAATCCA AAGCATGACC ATCAGGCACT GCTTCTCCAA CACTCTCGTC CTTAATCTGT 1200 GCCAGGCTTG TCCTTGGTGC TGGGACCCTG GGGTTTCAGC TCCAGGGAGC GTTCTCTGCC 1260 CCTTGGTAGG CAGCCTCTGG CCAAACCCTT GATGGAACTC CAGCCTGCTC TACTGTGTCC 1320 CTGGCTGCGG GGACTGCGTA TAGCCTGGCC CTCAGTTTCC TCAACAGTGA AATAGGGACA 1380 TGGTCACCTT CAGGGGGCAG TTATAAGGCT CAGGGTAGGG TATGTTCCAG GCATGGCTAT 1440 GCCGCACTGT TTATCACCAA GAGGGATGGA AGGTCTGTCC CAGAGCTGCC AGAGGGGAAC 1500 GGGTCAGCCA CCCCTGACCC ACCCCTTTGT GACTGGCTCC CTGGGCTTCT GTGCTGTCCC 1560 CCACTTGACT CTGCTCGCAG ACAGCTACAA TGGGGAGCCC CACGGGCTGC CCTTCACATT 1620 GTAGTCTAAG TGAGTGGAGC TGTGTGCCCG GCTCTATTCC CCAGCCTGGT CTCCCTTGCC 1680 CACCTCATCG CTGGTCCTGG CCCCTCCCCA 1710
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