Tag | Content |
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EnhancerAtlas ID | HS091-16291 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:11013400-11016020 |
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) |
CEBPA | MA0102.3 | chr16:11015886-11015897 | TGTTGTGCAAT | - | 6.14 | NFIC | MA0161.2 | chr16:11015864-11015875 | TACTTGGCACA | + | 6.32 | Zfx | MA0146.2 | chr16:11014968-11014982 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09716 | chr16:11014871-11016221 | CD14 | SE_10278 | chr16:11015248-11016093 | CD19_Primary |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I010920 | chr16 | 11014541 | 11019040 |
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Enhancer Sequence | TCTCACCCAG GTTGTAGTGC AGGGGTGCAA TGATGGCTCA CTACAGCCTC GACTACCTGG 60 ACTGAAGCGA ACCTCCCACC TCAGCCTTCC AAGTAGCTGG GTCCTATACC CTCCTGAGCC 120 TTGTTAATTT CTTCCCAGCA TGATCACTGT TTTACAATAT TTTATTTATG TAGGTGCTTA 180 CTTCTTGCTA TGCAAAGAAA CTCAGAAGCA AAAATAGAAT CTGTCTGGTT CATAATTGTG 240 CTAAAAACTA GAGATACAAG TATGAACTAG ACAGATGTCG TTCTTGCTTT TGAGTTTCTT 300 TGCGTAGTAG GAATTAGGCA CATACATAAA TAAAATATTG TAAAACAGTG ATTCATGCTG 360 GGAAGGAAAC TAACAAGCCC CAGGAGGGTA CAGGACTTCT GGGGAGATGA TTCTTCCGTG 420 GGAAGCTCTA GGGGAAAAGG ACTCTAGGAA GAAAGAACAG CAGGTGCAAA GGCCCTAAGT 480 GGGAAAAGGG GCTGTGTTTT AAGGGTCAGA AGGGCCACTG TGGCTGTGTG TAGTGAATGA 540 GGGACAGAGG CTGGGCAATG GTGGAAGTAG GGGAGGTCAG GGGAATCCAG ATCACACAGG 600 GAGGCCCTTG TGGGTCACAA GAGGTATTTG CAGTTTTTCA GTGTGAATGG AAAAGTAGGT 660 GGGCCTGGGA AGGCGACACT TGATCTGATT TACACTTTTC TTTTTTCTTT TCTTTTCTTT 720 TTGAGACCAA GTCTCACTTT ATTGCCCAGG CTAAGGTGCA GTGGCATGAT CTCAGCTCAC 780 TGCAAGCACT GCCTCCTGGG TTCAAGTGAT TCTCATGCCT CAGCCTCCCA AGTAGCTGGG 840 ATTACAGATG CCCGCCACCA CACCAGGCTA TTTTTGTGTT TTCAGTAGAG ACAGGGCTTC 900 GCCATGTGGC CCAGACTGGT CTTGAAATCC TGGGCCCAAG CGATCCACCC ACCTCAGCCT 960 TCCAAAGTGC TGGGATTACG GGTGTGAGCC ACCATGCCCA GCCTGATTTA CCCTTTAAGA 1020 AACATCATAT TTCATGGAAT CTAAGATGCC ATCCATTGTA AGACCCCAAT ATGAGGCCAA 1080 AATGCAAACT GTGACACGCT ATTGGTTATA AGACACATCC TGATCTCAAT GATATTCAAA 1140 TGGTGACATA TATGTCTTGG CATCGATGAA ATATGGTCAG ATTACTCTCC CTGTGGGGTG 1200 GAGGAAGGGT CTCCAGGGTT CAGAGATTGC AAAACCCCCA TCTAGTTTCT GCACTGGTAC 1260 CGGCCGACCC GTGATGTGAG TTGATTTAGC CTGAATCCAC TTGGCAGCAG TGTAAACCTG 1320 CTGCATTTAT TTATTTTTTT CTTTTTTTTT CGAGACAGAG TTTCGCTCTT GTTGCCAAGG 1380 CTGGAGTGCA GTCTCAGTTC ACTGCAACTC CGCCTCCCGA GTTCAAGCAA TTCTCCTGCC 1440 TCAGCCTCTC AAGTAGCTGG GAGTATAGGC ATGTGCCATC ACACCCGGCT AATTTTGTAT 1500 TTTTAGTAGA GACGGGGTTT CTCCATGTTG GTCAGGCTGG TCTCAAACTC CCGACCTTAG 1560 GTGATCCACC CGCCTCGGCC TCCAAAGTGT TAGGATTACA GGCGTGAGCC ACTGCACCTG 1620 CTGCTTTTAT ATGCAGCCCT GCAAGGGAGT TCTGAGGCTG AATCATGGCA AAGTCATGGC 1680 CCTGAAATCA TACCCGCAGC AGCACCTGAC CTGTTAAAAG GCTGCTTGGT GTCGAGTAAA 1740 CAGCTGAAGT TGGCATCAGT GACACTCATC ATGCTATTTT CACTGCTACT AATGCTGGTT 1800 GTGAATATGC TGCAGAAACT GGAGCTGGTC CAGTGACTGG CTTTTTCTCT TCCTGCCCCC 1860 AGTGCTGGTC ACACCCTCTA TGTTAACTCA TGCGACCCTC ACCAATGTTC CTGTGATGTA 1920 GTCAGAACCA TAGCTAACAT TTAGTTCATT CTAGGCACCA AGGCATGTTC TAAATGTTAT 1980 ATCAGCATTG ATTCATTTAC TCCTCCCCAC AATGACTCTA TCATGCCCAT TTTACAGATG 2040 GGCAAACTGA GTCTCAGAAG AGTTGAGTAG CTTGCCCAAG GTCACATAGG CAGTAAGAGG 2100 CATAGCTGGG ATTTGAACTT GGGAAGTTGT TCTGACAGTT TCCACACAGT AAGGCAAGAA 2160 ATGACTTCCT TTTAGTCCTG CTGTTTTCCT GGGCTCACTG TTTGACCACA GAGAAGTGGT 2220 CTCAACTCTC TGGGTCTTGG TTTGCCTGTC TTTAAAATGG GGCAGTAATC CCAGTAGGTG 2280 GTGACTCCCA CGGGGCTGAC CTCCAGGCTG CAGGGGACAC TGAGATCCTA GAAGCAATCA 2340 CCACAGCCCT GAACAAGAGA ACTAGTGGGA CCTGGGGACA GAAACTTTGA GCAAGTCACT 2400 TATTCATTCC TAGCCTCTAT TTTCATATCT AGAAAATGGG AACCATCCCA ATGGCCTATG 2460 TAAGTACTTG GCACAATGCC AGGCTCTGTT GTGCAATAAA TATTGATTCC TTCCCCCAGG 2520 GATAGTGGGA CCAGGCTTTT TCTGGAATCT AGGGATGGTG GCTTCTGGAA GGCTGACCAT 2580 GCACAGGCCT CCAATCCCTC CCCCTGGCCT CTGTTTCCGA 2620
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