Tag | Content |
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EnhancerAtlas ID | HS091-16913 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:28986880-28989220 |
Target genes | Number: 19 | 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) |
EWSR1-FLI1 | MA0149.1 | chr16:28987704-28987722 | TTTTTCTTCCTTCCATCC | - | 6.19 | EWSR1-FLI1 | MA0149.1 | chr16:28987712-28987730 | CCTTCCATCCTTCATTCA | - | 6.46 | EWSR1-FLI1 | MA0149.1 | chr16:28987708-28987726 | TCTTCCTTCCATCCTTCA | - | 6.8 | Zfx | MA0146.2 | chr16:28988400-28988414 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 28988745 | 28988818 | chr16 | 28987788 | 28987909 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I028977 | chr16 | 28989141 | 28989290 |
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Enhancer Sequence | GAGTGGGGAC CACTCCTGGT CACACAGCCG CTCCTCCTTC TGTTCTGTCT CAAGTGGGGC 60 CACGCGCTGG CCTGTCTAGG GGCTCATTAA TGGAGGTTTT GTGGCCAGTT AGGGGAGGTG 120 ATGGCCCTGA TGTTGCTCGG GGGTCAGCGG GACACCACAT TTAAAGAGGG AGTCAGTTTA 180 GTATAACTAA GTATAACTTC ACCCAGGTGA AGACAGACCT GGGTTTAAAT CTCAGCTCTT 240 CCACTTATTG TGTGATGGTA GGCAAGGCAC TCAACCTCTC TAAGCCTCAT TTTCCTTGTC 300 TATAAGATGG AACAAGTAAT AACACGAATC ATCTCTTAGG ACTGATGTGA AGATTAACTA 360 AAAGATTGTC TGTGAAGGGC CTAGTGCAGT GTTTGGCACA TGGTAGACAC CCAGTAAATA 420 ATGGCAGGAG GGTTGGGTGT GGTGACTCAC GCCTGTAGTC CCAGCACTTT GGGAGGCCAA 480 GATGAGTGGA TCACTTGAAG TTAGGAGTTC AAGACCAGCC TGGTCAACAT GACGAAACCC 540 CATCTGTACT AAAAATACAA AAATTAGCCA GGCATGGTAG CGAGCGCCTG TAATCCCAGG 600 TACTTGGGAG GCTGAGGCAT GAGAGTTACT TGAACCCGGG AGGCAGAGGT TGCAGTGAGC 660 CGAGATCGCA CCACTGCACT CCAGCCTGGG TGACAGAGCG AGACTCCATC TCATAAATAA 720 ATAAATAAGT AAAGGCAGGA GAGGGTGTCT GGAATGGGGA GAGGTGTGTT TTACTTGTTC 780 ACAACTTTGG GACTTGTGGG AGAGGCAAAG CTAGAGCCAA GCCCTTTTTC TTCCTTCCAT 840 CCTTCATTCA TTTCTCAACC ATTTCTGAGT ACTCATTGTG TGCCAGGCCT GGAGGAAGTG 900 ATGATTACAC CTGTAGGACT TTGCGAAGAA CTTTTATGCC CCTTGTCTTC TAATCCTTCT 960 ATCAGTCAAA AATAGGTGTT ACTGTTCCTA TTTTATAGAG GAAGTAGGTA GTGATATCTA 1020 CAGCTTATAA AGAAACTGAG GCTTGGAGAA GAGTTAAGAC TTGCCCAGGG TCACACCACC 1080 AGTTGGAGGC GGAACAGGAA TTTGAAACCA GGTCTTGCAG TGTTCTTTTC TCTACTCCAG 1140 GCCAATGAGG AACTGGAGGT ATTTGAGGTG AAGTCTGGAG CAATGAGAAT GGGATCATAG 1200 GGCAAGGTCT TCAAACCTCT GAAGAGTTGT TGAGTTAGAG CAGCAGCTCT TTCTAGGCAG 1260 CCGGATTTAT TCACTCTCTT CACATGCTTA TTGAGCACCT GTTTTGCACT AGGCTGTGTG 1320 TTAAGTAAGT GAAAGAAACA CAGTCATGGC CAATACAGGC AAGGACCTTG CCTTGGGAGC 1380 TGATAGTACG CTATGCATGA GGCAGCAACA GCCAGTAAAA CGCTAAACTA AAGTGGGACA 1440 GTTTTCCCAT AGGGATAAGT GTTATGTAAC AGAAAACAGT CCAGGCGCTG TGGCTCACAC 1500 CTGTAATCCC AGCACTTTGG GAGGCCGAGG CGGGTGGATC ACGAGATCAG GAGATTGAGA 1560 CCATCCTGGC TAACATGGTG AAACCCCATC TCTACTAAAA ATACAAAAAT TAGCTGGGCG 1620 TGGTGGCACG CCCCTGTAGT CCCAGCTGCT TGGGAGGCTG AGGCAGAATT GCTTGAACCT 1680 GGGAGGCGGA GGTTGCAGTG AGCTGAGATC GCGCCACAGC ACTCCAACCT GACAACAGAG 1740 CGAGACTTCG TTTAAAAAAA AAAAAAAAAA AAAAGAGAAA AAAGTAAATG TGAGAGTCAG 1800 GTACTGGATG TGTGCTCACC TGGGCAGCAT GCTTCACCCT TGGCCCTGGG CAAGTATCTG 1860 AGCTGGAACC TGAAGGAACT ATGCTCTGTG AAGTTTCAGG GGGAGAGGAG AGAATGTCCT 1920 TGATAGAGGA GGCAGTAGGT GCCTAAACCC CTAGTGGTAT TGGCCTTGAC AATTGGGCCA 1980 TTGGGATGCA GACAGAGGAA GGGAAAAAGG CTGGCCATGA GTGTGGAGAG GTAGGCAGGG 2040 CCTAGATTGG ACAGGGGCAT TGTGAGCCAT GGTATGCATG GAGTTTGGAG CTTGTTTTGG 2100 CTAGGTGGAA GGAATTGACA AGTAGTGGGA CCATCCATTA TACAATGGGA AATCTGGAAA 2160 GGTGTTCAAG ATGGAGCTGG ACCATCCGCC TGACAGGAAG CTCTGATGGG CTTCAGGCTG 2220 GGATGTGGGG GTGTTGTGAA TTCTGTAAGG AGAAGGCAGG CATCTCCTGT GCTTTAGTGG 2280 TTCCAGCTGG GGTGGGAGTG GGAGGTAGGG GTACCTGGGC TGAGCTGTGA CTCTCTGCTT 2340
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