Tag | Content |
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EnhancerAtlas ID | HS091-19930 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:42449790-42451720 |
Target genes | Number: 20 | Name | Ensembl ID |
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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) |
MEF2A | MA0052.3 | chr17:42450308-42450320 | TTTATTTTTAGA | - | 6.07 | Nr2f6(var.2) | MA0728.1 | chr17:42451492-42451507 | CGAACTCTTGACCTC | - | 6.24 | TBX20 | MA0689.1 | chr17:42451708-42451719 | CTTCACACCTC | - | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I044374 | chr17 | 42451541 | 42453868 |
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Enhancer Sequence | CCTGGGGGTA CACGGGGGCC AAGGTCAGGG TATACAGATG ATTTGCTGGC CCCAGAGCAC 60 ATGTGAGGAA GTATGCTAGC TATGAGCACC TCCCTGGACC AGCGCAGAAC ATGAAGCCCA 120 CTGTACTCAC AAATGGATGC CTTTTGACAT TTAGAGATAA TGCATGGAAC GAATTGTTGG 180 GTTTTTGTTT TTTCTCCCCT GAGTTTTTAT TTTTTTCTTT TTTTTAGAGG GAGTCTCACT 240 CTGTCACCCA GGCTGTAGTG TAGTGGCTCG ATCTCGGCTC AGTGCAGCCT CCACCTCCCG 300 GGTTCAAACA ATTCTCATGC CTCAGCCTCC CGAGTAGCTG GGTTTACAGG TGTGTGCCAC 360 CACGCCCAGC TAATTTTTAG TAGAGACAGG GTTTCACCCT GTTGGCCGGG CTGGTCTCAA 420 ACTCCTGACC TCAGGTGATC TGCCTGCCTC AGCCTCCCAT TGTGTTGGGA TTACAGGCAT 480 AAGCCACTGT GCCCGGCCTC TGAATTTTTC TTTTTTATTT TATTTTTAGA GACAGGGTCT 540 TTCTGTTGTC ACCCAGGCAA TCCTCTCACC TCTTAGCCTC CCAAGTAGCT GGGACTACAG 600 GTGTGGACTA CCACACCTGA CTAATTTTTT TTAAAAAACT TTTTTGTAGA GATGGAGTCT 660 CACTATGCTG TCCCAAACTC CTGGCCTCAA GTGATCCACC GCGCCTGGTC CCCACCTGGA 720 ATTTTTCTTT TCTTTTCTTT TGAGATGAAA TCTCACCCAG GCTGGAGTGC AGTGGCACAA 780 TCTTGGCTCA CTGCAACCTT CACCTCCCGG GTTCAAGTGA TTCTCCTGCC TCAGCCTCCC 840 GAGTAGCTGG AAGTACAGGT GCCTGCCACC ACGCCTGGCT AATTTTTGTA TTTTTAGTAG 900 AGATGGGGTT TCACCATGTT TGTCAGGCTG GTCTCGAACT CCTGACCTCA TGAACCGCCC 960 ACCTCGGCCT CCCAAAGTGC TGGGATTACC GGTGTGAGCC ACCACGCCCA GCCTGGAATT 1020 TTTCTTATAC TGAAGTTTGT GTCTGCATGA CTCGAGCATA TGATGATATG TATTTGATTA 1080 TTGTGGGTCT AGTGCGTGGT TTTCCCTAAA AGCACCATGT CTTCCCTTCA GTGTGCTTGA 1140 GACTCCTCCA GGTGCAGAGG AGCGAGTGAC CCTCCAGGGC CACATAGGAA GGGAGGAATA 1200 GGGTCTAGAC CAATCCTTGG GCCTCTTGCC TCACTCAAGG GGAAGGGCAG GGCTAGGAAG 1260 AAGTGCATCT TGTCCTTGAG ACCAGCCAGG AATTCCTGAA GGCAGGACTT ACACCCTCTA 1320 TACCCTCTAT ATCCTCTGAA TCTTTTTGGT GGCAGGGGTG TCTAAAGGCC TCAGAATTTC 1380 AGGTGCTATC CTTTCCAGTG GTATGTGTCT GGAAGGGTTC CCAGGAGAAT GACATTTTTG 1440 TGTTTGTTTT GCCTTTTTTG CTCTACTAGA GAAAGACATT CTATTTTTTT CTTTTTTTTT 1500 TGAGATGGAG GCTCGCTCTG TTGCCCAAGC TGGAGTGCAG TGGTGTGATC TCGGCTCACT 1560 GCAACCTCCG CCTCCTGGGT TCATGCAATT CTACTGCCTC AGCCTCCCGA GTAGCTGAGA 1620 TTACAGGCAT GTGTCAACAC GCCCGGCTAA TTTTGGTATT TTTAGTAGAG ATGGGGTTTC 1680 ACCATGTTGG CCAGGCTGGT CTCGAACTCT TGACCTCAGG TGATCTAAAC GCTTTGGCCT 1740 CCCAAAGTGC TGGGATTACA GGTGTGAGCC ACCCCACTGG ACCGAGAATG ACATTCTAAT 1800 AGTGGAGACA TAGACCCCTG GTCCCTGGAT TACCCACTTG GGTGGGCCAC CATCTCTCCT 1860 TGACTCCCTG TGAGGCAGGG CAGAGCCAAG CCTGTGCCCC GCTGGGGACT CCACCGTCCT 1920 TCACACCTCA 1930
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