Tag | Content |
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EnhancerAtlas ID | HS091-21187 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:73999480-74001370 |
Target genes | Number: 36 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr17:74001147-74001158 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr17:74001147-74001158 | GGGTGACTCAG | + | 6.02 | Nr5a2 | MA0505.1 | chr17:73999562-73999577 | GAGTCCAAGGCCAGG | + | 6.69 | ZIC1 | MA0696.1 | chr17:74000938-74000952 | CACCACAGGGGGTC | - | 6.49 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_24501 | chr17:73999053-73999875 | Colon_Crypt_2 | SE_24501 | chr17:74000077-74000407 | Colon_Crypt_2 | SE_24501 | chr17:74000678-74001383 | Colon_Crypt_2 | SE_27115 | chr17:74000627-74002264 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I076002 | chr17 | 73998813 | 74002281 |
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Enhancer Sequence | TAGGTGCATG TGGGCTCCAG CTGCTGCTCC GACTACAGTT TCCCCTCATC AGCCAGCCTC 60 TTACATAACC CTGGCACTTT CTGAGTCCAA GGCCAGGGTC TCTTTCCTGA CCTTTGTACA 120 CAACTGGCTT GGGTATACTG ATTGTTCAAC CCGGAAGCCT CCCCCAGGAT AAGTGCAGTA 180 TTTATCTTCC CTGTGAAAGT GGCGCTCATT GAGTTAGCTC TGTCTTTATG CTGTGCTACA 240 CGCCCTTTTT CCCTAGTTGT CTTGTGTGTT TGGTTATTCT ACTTTGTGGA CATTACTGCT 300 CCATCTAAGC TGTATGCCTC CCCAGGCTGG GGCCATACCT TCTTTTCTTT TCTTTTTTTT 360 GAGATGGAGT TTTGCTCTTG TTGCCCGGGC TGGAGTGCAA TGGCGTGATC TCAGCTCACT 420 GCAACTTCTG CCTCCTGGGT TCAAGTCATT CTCCTGCCTC AGCCTCCCGA GTAGCTGGGA 480 CTACAGGTGC CTGCCACCAC GCCCAGCTAA TTTTTGTATT TTTTTTTTTA GTAGAGACAG 540 GGTTTCACCA TGTTGGCCAG ACTGGTCTTG AACTCCTCAG GTGATCTGCC CACCTCGGCT 600 TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACTGTGCCC GGCTGGGGCC TCTCGTTCTA 660 CTGCCTGGCT GTTCCCCTGT GACTCCTACA GTGGTCAGTC TTCAGAACAG GCTGTTCCCT 720 ACTGCCTGGG CCCATGCCAC AGTTCTCACT CACCCCTCCT GTTGGTGTCT TGAGCTGACC 780 CAGGCCGGAC TGCCCAGGAA GTCTCTGGCA GAACCGTCTG TTTTTTTTTT TTTTTTTGAG 840 ACAGGGTCTC AGTCTGTCAC TCAGGCTGGC GTGCAGTGGT GTGACCATGA CTTACTGCAG 900 CCTTGACCTC CCAGGCACAA GCGATCCTCC CATCTCAGCC TCCTGAGTAG CTGGGACCAC 960 AGGTATACGC CACTATGCCT GGCTACCTTT TGTATTTTTT TTGTAGAGAC AGCATTTCAC 1020 CACGTTGCCC AGGCTGGTCT CGAACTCCTG GGCTCAATTG ATCCTCCCAC CTCAGCTTCC 1080 TGAGTAGCTG AGACTATAGG GGTGCACCAC CATGCCCAGC TAATTTTATT TTTGTAGAAA 1140 TGGGGTCTCA CTATGTTGCT CAGACTGGTC TCGAACTCCT GGGCTCAAGC GATCCTCCTA 1200 CCTTGGCCTC TCAAAGTGCT GGGGGGATCA CAGGTGTGAG CCACTGCGCC CGTCCACTGT 1260 CCATTCTTGC CCACAAAGTC TTGGAGCCAC ATTTCTCTCC TTAATCTGGT GTTGAATGAG 1320 AGGAAGGTGG GTCAGTATTT TCATCTTCAG GCTGTGTGTC CAGCTCTCCA GAAGTCTCTG 1380 TGTGTTGTGT ACCCGCCCAA TGGCAGCAGG ACGGCACAGA CTCCAGCCAA GGCCCCGAGC 1440 CCTCCAGCTG GGCTACTCCA CCACAGGGGG TCCTTCCACA TCCTGTCTGG GTTTAGGGAC 1500 TCTAGGGCAG AGGGCTGGAC AGGTTTGGCC TCTTGGAGTG TCAGTCCCTG AGCCCCCACT 1560 CAGTGTTCCT CCCTGGACAG CTTCAGTCCC CTGCTTCCTG ATACGTGGGG TTCTGTGCTC 1620 TTCCCAACTA GAAGCAGGCT GGGACCTGGG ACCCTCCCCG AGAAGGGGGG TGACTCAGCT 1680 TCAGTGGCCT GAGGAGACCT GGGTGACTCG TTAGGACTGT CCAGATTCCA GGAGTGTCCG 1740 GAACTGGCTG GAGAGCTGGG AGGTCATGGC TTCATGCGGT TCTGGGTTTG AGGGCAGCCA 1800 ATTTGGGGCC CAGGCCCTTG ATCTGGGACC TGGGAGGGGA ATTTCTCACC CCACCCTGGC 1860 TGCACCCAGA CCACATCTTC TTCCTTCTTT 1890
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