Tag | Content |
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EnhancerAtlas ID | HS091-36344 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr4:9996180-9998400 |
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) |
GATA2 | MA0036.3 | chr4:9997410-9997421 | ACAGATAAGAA | - | 6.14 | Gata1 | MA0035.3 | chr4:9997410-9997421 | ACAGATAAGAA | - | 6.62 | ZNF263 | MA0528.1 | chr4:9998099-9998120 | GATGGAGGGTGGGAGGAGGGA | + | 6.09 | ZNF263 | MA0528.1 | chr4:9997984-9998005 | TTCCCCTCCCCTCCCTGCTCT | - | 7.34 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_34108 | chr4:9997360-9998006 | HCC1954 | SE_53020 | chr4:9996030-9996905 | Small_Intestine | SE_53020 | chr4:9997188-9999152 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I009993 | chr4 | 9995466 | 9999128 |
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Enhancer Sequence | CCTTTTCCTT TTTTTTTTTT TTTTTTGTTG CCATGCCAGT GAGGGTAGTA AAGCTACTTT 60 CATTGCCCTC ATTTTATAGG TAAGAATAAT GCTGGCTGAG AAGTGAGGTG TCAAAGTCCC 120 TTGTAACACA CCTGATACAC AGCAGAGTCA GGACTTGCTG AGCCACGGCA TTCTGACCCG 180 ATTCTAGTGT TCCTTTTCCT ATTCCATCTG CATGGGTTCA GAGCCTCCTT GAGGAGCAGC 240 CTTGGGGTAT AAATGCCACG GTCAGGTATA AAGCAAGGAG ACATCACAGG CCAGATCCTG 300 GGGCATGGGG AGTGACTCCA TCCCACTAGG ACAAGCAAGA GGACCATGGG CAGGGTCTGG 360 CTTGGGCAGG AGGCTTAGTG ACCATGCCTC AGGGACCCTG GCCAGTGATG CCAATCTGAG 420 TGCCAGCCTG TTGTCAAACA GTCATGGTTT TACAGTACAT TCCCAGCATT GGGAATTGGC 480 CCCTAACTAA GATCTGCTTG GCATAGTGGA AAGATCATGA TTCCAGCCTA AGCTCAGCCA 540 CAGTGCAAGC TAGCTAAGCT TGTGCAGATG CCCTCACCTC TCTAACCTCC CATTCCCCAT 600 CTACAGACCC CACAGCAGAT AGAAAATTAA ACAAGAGAAT GTGTGAGTGG CTGGAACCTT 660 GAAGGACCTC AGACAATGGC ATCTCTCACT ACATCATGCA GTAGTTGTAT TTCCAGGCCC 720 TGAATTCCCA TTAATTACTG CTCTGAAAGT GGGCTTGGGG ACAAGGAAAA TGTCAGCACC 780 TCCCCTACCT CACAGGTATC ACAGACCCTC ATAAGCACCA CTTGGATGTT TTCAGGGTGG 840 CTTCCTGTCC CATCTTTTAG AAATCTTGCT TTGAAACATC GTCAACTCTA GTTTTCTCCT 900 TGTTGGGCTG TGAGGAAGAA TGTAAAGGAT TCGGTCATTT CAGATTGTGA AATGGGCTCC 960 TTCTTAATCG GGTTTCTGTA ATCCCATGGT CTGAGGAGAT TTTCTGGAGT CTGATAAATC 1020 TCCTCTTCAA CTCACGTCAA TGCAATAAGG AGGTTAGTCG AGTACTTACT AGGTAGTGAT 1080 GTCAAGGTGA TGATGAGGGA AATGCCAAAT AATGTGGTCA ATGACAAGAA TTTTTATTTA 1140 TTCAGCTACA ACTCATGGCC ATTCTCCTTC CATTCATTTG GTCTAACTCT TGTAACATTC 1200 CCTGCAGGTA GAAACTATCA TCCCTATTTT ACAGATAAGA AAATTGAGGC TCAAATAAAT 1260 TAAATGATTT GGCCAAGGGC ACACAGCTAG TAAGTGGAAG ACACATGATT CAAGTTAAGA 1320 CACGAATGTT CTGGCCCCAT CAGATTGATG TGACGACTCC TCCATCACTT GGAGAAGCTC 1380 TACTCTTTCC ACACACTGCT CACTGGCTCC CAGGATGCTG TTGTTATGAA CAAGAATACA 1440 GAGAAAGCAT TGTTTGTGGG GATTCATTGA TAAGTCAATC TGCTCTGAGA GAAGGATTCC 1500 TGTCTAAAAT AAGTGAGGAA TGAGGCTCAC AAGGTCAAGT GAGCTGATTG GAGAGGGCCT 1560 GGGTAGGAAA GGCTGATATG AAGTTTTTGA TTCTCACTGC TTCCTTATTT GTAATGTAAA 1620 TGATCTGAAA TGACCTAAAT GTCTCTCAGT CAGGGAGTGT GGCTAAATAA ATGATGAGAC 1680 AGCCATATAG TGGAAGACTG TCTAAGCAGT CAATTTTCTG GAAAAGCAGA TCTGTATGTA 1740 CTTACGTGGA ACAATTTCCA AGGCACTGCA CTGTGTTTTC CATTTGCCCC AACACCCAGA 1800 TCAATTCCCC TCCCCTCCCT GCTCTGCTCT ATGCCCCGGG AGCATCTCCT GGATGGCAAC 1860 ATGACTTCCT GGTTTACTGG CTTTCACATG GGTGTGACCA GTGTGCACCT CTGCAGCAGG 1920 ATGGAGGGTG GGAGGAGGGA GGGGTCAGGG CATTTCTTCC CTGCTCCTCC CCCATGTGGG 1980 TGCTGTGGCT CTGACACAGC CCAGTCCCTA TACGCTTCTG CTGCTGCTCA TCAGCCTGCA 2040 GTCCATGGCT TCAGTTATCT TTGGACCTTG GTCTCTGATT TCTTCCCCTT TCCCCTTTGG 2100 GCATTTGAAT CTCTCCAGTT GAACTGCCTG AGTGGAGTTC TGTTGCCTGT CAGGACCCTG 2160 ACAATGACAC AGATATATTA TGAACATGGA GGGCACCCCC AGATAGAGAC AGCCTCCTAC 2220
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