Tag | Content |
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EnhancerAtlas ID | HS091-19322 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:27776180-27778470 |
Target genes | |
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) |
EWSR1-FLI1 | MA0149.1 | chr17:27777036-27777054 | TTTTTCCTCCTTCCTTCC | - | 6.18 | EWSR1-FLI1 | MA0149.1 | chr17:27777040-27777058 | TCCTCCTTCCTTCCTTTC | - | 7.55 | HNF4G | MA0484.1 | chr17:27777348-27777363 | TGCACTTTGACCTCT | - | 6.33 | Hnf4a | MA0114.3 | chr17:27777346-27777362 | CTTGCACTTTGACCTC | - | 6.67 | NR2C2 | MA0504.1 | chr17:27777348-27777363 | TGCACTTTGACCTCT | - | 6.3 | RARA | MA0729.1 | chr17:27777610-27777628 | CCTTGACCTCCTGAACTC | - | 6.28 | SREBF2 | MA0596.1 | chr17:27777160-27777170 | ATGGGGTGAT | + | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I029450 | chr17 | 27777301 | 27777450 |
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Enhancer Sequence | TGAAGTTTGT TTTTTTAATA GTTTGATTAA TTGAAAATTA ATACTTTATA TGGAATTTAG 60 TTCAGCCTAC TCAGTTTAGG GATGAGAAGT TAAGTGACTT TGCTATGGTC ACATATTCTT 120 GGAAGAACTG TGATTAAGAC TGCTCCAGGG AACTTCTAGA ACAGGGAAAT TGGTAAAAGT 180 ATATGGGGCA GCCTTGGATA TATATTAGAA ATTGAATACA AATTAAGAAT TTATATATTT 240 TTATTGCAGT GTGGTGTTAA TTTAGGGGGG TACAAAAGAC ATATAAATGT ATTTTATATA 300 GTTACAAAGA AGTTTTCTAG CAAGAATTAA AATTGCTTGT TACTTGACAA GAATTGGATG 360 GAGCTGTTTT TTTCTCTTAA AAGTCTGATG AAATCAGGCC AGGTGTGGTG GCTTATGCCT 420 GTAATCCCAG CACTTTGGGA GGCTGAGGCA GGCAGATCAC TTGAGGTCAG GAGTTCGAGA 480 CCAGCCTGGC CAACATGGTG AATCCCCATC TCTACTAAAA ATACAAAAAT TAGCCGGGGG 540 CGGTGGTGCG TGCCTGTAGT CCCAGCTACT TGGGAGGCTG AGGCAGGAGA ATTGCTTGAA 600 CCTGGGAGAT GGGTGTTGCA GTGAGCTGAG ATTGTGCCAT TGCACTCCAG CCTGGGTGAC 660 AGAGTGAGAC TCTGTCTCAA AAAAGGAAAA AATAAAGCCT GATGAAATCA ATTTTGGAGT 720 TTTTAAAAAT TGTTGAATTT GAACAAGTTA AAAGAAAATA GCTAACACTT ACTGTAGTGC 780 TTATTACTCC AGAGTATTAC TCTATGCTTT CATTTATTAA CTCATTTAAC CCTCCTGATT 840 ACACTGTGAA GTAGATTTTT TCCTCCTTCC TTCCTTTCCC TTTTCTTTTC TTTCCTTTCC 900 TTTTTATTTC CTTTTTCCTT TCCTTTCCTT TCTTTCATCT AACAAACAGG GTCTCTCTCT 960 CTTGCCCAGG CTGGAATGCC ATGGGGTGAT CATCACTCAC TGTAACCTCG AACCTCTGGG 1020 CACAAGTGAT CCTCCCACCT CAGTCTCCCA AGTAGCTAGG ACTATAGGAG CACACCACAC 1080 CACCCAGCTA ATTTTGTAAT TTTTTTGTAT TGGAAGATCT TGCTGTGTTG TCTGAGCTGG 1140 TCTCAAGCTC CTGGCCGCAA GTGATCCTTG CACTTTGACC TCTCAAAATG CTTGGATTAC 1200 AGATGTGAAC TTTCACACCT GGCCTATAGT CATTTTACAG ATTAGGAAAA TGATACTACC 1260 TAATTTCAGA ACTAGTGTTG CTGGGATTCC TATCCAGCAG TGTCATTCCA GAGTCCAGGT 1320 TCCAAAGCCT CTTAATTATG ACATCCAGTT TTGTTTTGTT TTGTTTTGAG ACAGGATCTC 1380 ACCCTGTTGC CCAGGCTGGA GTGCGGTGGT GTGATCATAG CTCACTGCAA CCTTGACCTC 1440 CTGAACTCCA GTGATCCTTC CGCCTTAGCC GCCAAAGTAG CCAGGACTAT AAGTGCATGA 1500 CACCACTCTT GGCTAATTTT TTAAATTTAT TTTTGTAGAG GCAGGGTCTT ACCATATTAC 1560 CCAGGCTGGT CATGAACTCC TGGTCTCAAG CGATCCTCCT GCCTTGACCT CCCAAAGAGC 1620 TGGGATTACA GGCATGAGCC ACTGAGTCTG GCTATGACAG CCAGTATTAA AACTGGGTAA 1680 TCTGATATAA AGGAATTGAT AGGACAACTG CCAGGAAGTT TTCTGGTTAT CTGTATTTCT 1740 ACTTATTTAA TGAAACAGTT GATAAAGGGC ATATTTTAAT GTGAATCAGG TGAATCAAGT 1800 TTATGGAGAA ACAGTTGTCT GTGAAATACA TTACTTTCTC CCACTATATT TTTCTTTGAA 1860 TGTCTGTTAG AGTTGATTAG TACACTAGCA TACGGTATCT GAAAAGAAAA GAAGTTTCCT 1920 GTTGTCAGAA ATACTGTGGG CACATCTTGC GTTATTGTGT ATTTTTAAAA TAGTCTCTTT 1980 TATATTATCT TCTCTATTGA TGAGATGACT GCATCAGAAG TGGATACATT TTTAAGTATT 2040 GACTTAGAAA ACCTCCCAAG ATACAAAGAT TATCTCATTT TTTTAAAGTG CTGTATAGTA 2100 GGAATCTGTT TTTGAAGTAC CATGGTGTTC ATGATGATGA AACAGGTTTA GGAGCTACTG 2160 CAGTAGTACC CACACTGCCT TTTCAGTGAA ATTCTAGACA TGAGATAAAT TTGTAGATCA 2220 GTATATGACC TTATACTAAT TATTCTTAGC AGTTTTTGCC TTTTCTGACT TTTTTTTTCT 2280 ATTTTTCTAC 2290
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