Tag | Content |
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EnhancerAtlas ID | HS091-21438 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:78075690-78078350 |
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) |
ETV6 | MA0645.1 | chr17:78077727-78077737 | CACTTCCGCT | - | 6.02 | EWSR1-FLI1 | MA0149.1 | chr17:78077671-78077689 | GAAAGGGAGCAAGGAAAG | + | 6.44 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | TGAGACACCT GACGTCTGCC CCGCGCTGCC GGCGGTAACA TCCCAGAAGC GGGTTTGAAC 60 GTGCCTAGCC GTGCCCCCAG CCTCTTCCCC TGAGCGGAGC TTGAGCCCCA GACCTCTAGT 120 CCTCCCGGTC TTTATCTGAG TTCAGCTTAG AGATGAACGG GGAGCCGCCC TCCTGTGCTG 180 GGCTTGGGGC TGGAGGCTGC ATCTTCCCGT TTCTAGGGTT TCCTTTCCCC TTTTGATCGA 240 CGCAGTGCTC AGTCCTGGCC GGGACCCGAG CCACCTCTCC TGCTCCTGCA GGACGCACAT 300 GGCTGGGTCT GAATCCCTGG GGTGAGGAGC ACCGTGGCCT GAGAGGGGGC CCCTGGGCCA 360 GCTCTGAAAT CTGAATGTCT CAATCACAAA GACCCCCTTA GGCCAGGCCA GGGGTGACTG 420 TCTCTGGTCT TTGTCCCTGG TTGCTGGCAC ATAGCACCCG AAACCCTTGG AAACCGAGTG 480 ATGAGAGAGC CTTTTGCTCA TGAGGTGACT GATGACCGGG GACACCAGGT GGCTTCAGGA 540 TGGAAGCAGA TGGCCAGAAA GACCAAGGCC TGATGACGGG TTGGGATGGA AAAGGGGTGA 600 GGGGCTGGAG ATTGAGTGAA TCACCAGTGG CTTAGTCAAC CATGCCTGCA CAATGGAACC 660 CCGTAAGAAA CCACAGGGAT CAGAGGGCTT CCCGCCGGGT TGTGGAACAC ACCAAGGCAC 720 TGGAGGGTGG TGCGAGCAGA GAGCACAGCA TCACTGCCCC CACCTCACAC CAGGCCCTAC 780 GCATCTCTTC CATACGGCTG TCTGAGTTTT ATCCTTTGTA ATAAACCAGC AACTGTAAGA 840 AACGCACTTT CCTGAGTTCT GTGACCCTGA AGAGGGAGTC CTGGGAACCT CTGAATTTAT 900 AACTAGTTGA TCGAAAGTAC AAGTGACAAC CTGGGATTTG CCATTGGCCT CTGAAGTGAA 960 GGCAGTGTTG TGGGACTGAG CCCTTAACCT GTGGAGTCTG TGCTGACTCC AGGTAGTGTC 1020 AAGATTGAAT TGAATTGTAG GACACCCAGC CGTGTCCAGA AAGTTGCAGA ATTGATGGGT 1080 GTGAGAAAAA CCCTACACAT TTAATGTCAG AAGTGTGGGT AAAATGTTTC ACCCTCCAGC 1140 CCAGAGAGCC CTAATTTACC AGTGGCCCAC GGTGGAACAC CACGTCCGGC CGGGGGCAGA 1200 GCGTTCCCAG CCAAGCCTTC TGTAACATGA CATGACAGGT CAGACTCCCT CGGGCCCTGA 1260 GTTCACTTCT TCCTGGTATG TGACCAGCTC CCAGTACCAG AGAAGGTTGC ACAGTCCTCT 1320 GCTCCAAGGA GCTTCACTGG CCAGGGGCTG CTTTCTGAAA TCCTTGCCTG CCTCTGCTCC 1380 AAGGCCCGTT CCTCAGAGAC GCAGACCCCT CTGATGGCTG ACTTTGGTTT GAGGACCTCT 1440 CTGCATCCCT CCCCCATGGC CTTGCTCCTA GGACACCTTC TTCCTCCTTT CCCTGGGGTC 1500 AGACTTGCCT AGGTGCGGTG GCTCTCCCAG CCTTCCCCAC GCCCTCCCCA TGGTGTATTA 1560 CACACACCAA AGGGACTCCC CTATTGAAAT CCATGCATAT TGAATCGCAT GTGGGTTCCG 1620 GCTGCTCCTG GGAGGAGCCA GGCTAATAGA ATGTTTGCCA TAAAATATTA ATGTACAGAG 1680 AAGCGAAACA AAGGTCGTTG GTACTTGTTA ACCTTACCAG CAGAATAATG AAAGCGAACC 1740 CCCATATCTC ATCTGCACGC GACATCCTTG TTGTGTCTGT ACCCGAGGCT CCAGGTGCAG 1800 CCACTGTTAC AGAGACTGTG TTTCTTCCCC ATGTACCTCG GGGGCCGGGA GGGGTTCTGA 1860 TCTGCAAAGT CGCCAGAGGT TAAGTCCTTT CTCTCTTGTG GCTTTGCCAC CCCTGGAGTG 1920 TCACCCTCAG CTGCGGTGCC CAGGATTCCC CACTGTGGTA TGTCCGTGCA CCAGTCAATA 1980 GGAAAGGGAG CAAGGAAAGG TACTGGGTCC CCCTAAGGAC ATACGAGTTG CCAGAATCAC 2040 TTCCGCTGAC ACCCAGTGGA CCAAGCCGCA CCTTTATGCA GAAGTGGGGC TCCCAGCCAG 2100 GCGTGGTCAC TCCTGAAATC CCAGCACTTC GGAAGGCCAA GGGGGGTGGA TCACTTGAGC 2160 TCAGGAGTTC GAGACCAGCC TGGGTAACAT GGCAAAATCC CGTCTCTACA AAAATACAGA 2220 AAATTAGCTG GGTGCGGTGG TGTGTGCCTA CAGTCCCAGC TACTCAGGAG GCTGAAGTGG 2280 GAGGATTGCT TGAGTCTGGG AGGTGGAGGT TGCAGTGAGC CAGGATCTCA CCACAGCACT 2340 CTGGCCCAGG CGACAGCTGT TTGGCCTGTT TCAAGTGTCT ACCTGCCTTG CTGGTCTTCC 2400 TGGGGACATT CTAAGCGTGT TTGATTTGTA ACATTTTAGC AGACTGTGCA AGTGCTCTGC 2460 ACTCCCCTGC TGGAGCTTTT CTCGCCCTTC CTTCTGGCCC TCTCCCCAGT CTAGACAGCA 2520 GGGCAACACC CACCCTGGCC ACCTTACCCC ACCTGCCTGG GTGCTGCAGT GCCAGCCGCG 2580 GTTGATGTCT CAGAGCTGCT TTGAGAGCCC CGTGAGTGCC GCCCCTCCCG CCTCCCTGCT 2640 GAGCCCGCTT TCTTCTCCCG 2660
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