Tag | Content |
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EnhancerAtlas ID | HS108-16122 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:5414700-5417430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:5415122-5415140 | CTTTCCTTCCTTCCTTCC | - | 10.53 | EWSR1-FLI1 | MA0149.1 | chr17:5415130-5415148 | CCTTCCTTCCTCTTTTTC | - | 6.25 | EWSR1-FLI1 | MA0149.1 | chr17:5415142-5415160 | TTTTTCTTCATTCCTTCC | - | 6.33 | EWSR1-FLI1 | MA0149.1 | chr17:5415126-5415144 | CCTTCCTTCCTTCCTCTT | - | 6.84 | EWSR1-FLI1 | MA0149.1 | chr17:5415045-5415063 | CCTTCTTTCCCTCCCTCC | - | 6.94 | EWSR1-FLI1 | MA0149.1 | chr17:5415118-5415136 | CTCTCTTTCCTTCCTTCC | - | 7.37 | EWSR1-FLI1 | MA0149.1 | chr17:5415041-5415059 | CCTTCCTTCTTTCCCTCC | - | 7.87 | IRF1 | MA0050.2 | chr17:5415058-5415079 | CCTCCCTTTCTCTTTTCTTTT | + | 6.14 | IRF1 | MA0050.2 | chr17:5415069-5415090 | CTTTTCTTTTTCTTTCTCTTT | + | 6.59 | IRF1 | MA0050.2 | chr17:5415081-5415102 | TTTCTCTTTCTCTTTCTTCTT | + | 6.87 | IRF1 | MA0050.2 | chr17:5415098-5415119 | TCTTTCTTTCTCTTTCCTTTC | + | 6.99 | IRF1 | MA0050.2 | chr17:5415075-5415096 | TTTTTCTTTCTCTTTCTCTTT | + | 8.25 | SPI1 | MA0080.4 | chr17:5415133-5415147 | TCCTTCCTCTTTTT | - | 6.06 | SPIC | MA0687.1 | chr17:5415133-5415147 | TCCTTCCTCTTTTT | - | 6.38 | TCF7L2 | MA0523.1 | chr17:5416706-5416720 | TGGCTTTGATCTCT | - | 6.08 | ZNF263 | MA0528.1 | chr17:5415122-5415143 | CTTTCCTTCCTTCCTTCCTCT | - | 6.14 | ZNF263 | MA0528.1 | chr17:5415154-5415175 | CCTTCCTCTTCCTCTTTCTCT | - | 6.25 | ZNF263 | MA0528.1 | chr17:5415118-5415139 | CTCTCTTTCCTTCCTTCCTTC | - | 6.28 | ZNF263 | MA0528.1 | chr17:5415045-5415066 | CCTTCTTTCCCTCCCTCCCTT | - | 6.54 | ZNF263 | MA0528.1 | chr17:5415157-5415178 | TCCTCTTCCTCTTTCTCTTCC | - | 6.67 | ZNF263 | MA0528.1 | chr17:5415160-5415181 | TCTTCCTCTTTCTCTTCCTTT | - | 6.6 | ZNF263 | MA0528.1 | chr17:5415041-5415062 | CCTTCCTTCTTTCCCTCCCTC | - | 7.26 |
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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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| Number: 2 | ID | Chromosome | Start | End |
GH17I005511 | chr17 | 5414841 | 5414935 | GH17I005513 | chr17 | 5416862 | 5417624 |
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Enhancer Sequence | CAGTGAGCTG AGATTGCGCC ACTGCACTCC AGCCTGGGCG ACAGAGCGAG CCTCCGTCTA 60 AAAAAAAAAA AGAGAATCTG GATCCAAAGC GGACATGCAT GTGTGTCTCC CCCATCCCCA 120 CACACTTGTT TGTGTCTGGC CTTTCTCCTA CTCCAAGACT GGCTCCACTT CGGGGCTCGC 180 TGCCATGGAG ACGACTCCAG ATTTAGGAAT ACATTTCCTA GGCTTCCGGC AACTAACGTG 240 AGGACTTGCT GGGATGAGGG ACGGGGAGGT CTGCAGAAGG AGGCGGGGCA TGCGGGGGTT 300 GCGGGGCTTA GAGGGTTGGC GGAGCCCCTC CTCGCGTAGG TCCTTCCTTC TTTCCCTCCC 360 TCCCTTTCTC TTTTCTTTTT CTTTCTCTTT CTCTTTCTTC TTTCTTTCTC TTTCCTTTCT 420 CTCTTTCCTT CCTTCCTTCC TCTTTTTCTT CATTCCTTCC TCTTCCTCTT TCTCTTCCTT 480 TTTCTTTCTC TCTCTTCTTT CTTCTTTCTC TCTGTTGAAA ATTGTTTTTG ACCACACCCA 540 GATCATACTG ATATTTACAG TATAGTCCTG GCTACAAGGG AGCCCAGCTG TAACTTGTGA 600 AGTGGGCCTG GTTTAGAAAG TAACAATGAG GTGGTAACTA ATGACAGTAC TAGTTGTTAT 660 CAAAAATTAA CACCTTTAGG TATTTTTGTT TTGGGTTTTT GTGGTTTTGG TGCATCCACA 720 ATGTCTTCAT AGTCTGCACT TATTCCCTTT GCCCACAGAC CAACTGTGGC CATTCGATCT 780 GAATTCTCAC TTTCAGGGCA ATCTTTCTTT AAATGTTCCA CAGAGCCATG AAGTTGGCAA 840 CCACTACCAT CAGCATAGAG TCCTTTGGGA TTATCAGGAC AAGATCTAGA CAGGTGCCCC 900 ATTTCTCCAC AGACAAAACA TTCTGCAAAA GGACATTCGC CAAGAGGCGG GTCTACTTTA 960 GCCTTACACT TGGTTATTTC GTGATCTGTG GACCCACACT TGTAACATCT TCTAGTGCCC 1020 ATATCTTGAT TTTCAAGGGC GGCAGGGCAA TCCGCAATTC CACGACCAGG TTTTCTACAA 1080 TGGAAACACA CCATTGCATT TTTCTTTGCC CCTTGTCTTT TAAATCTTCT TACTTCCCAT 1140 TGACTGTCCT CTTGGAGGAA GGGTTGTGTG GAGAGTGGAG GTCTGCATGT GGTAAAGGAG 1200 ATGGGTGGGT GGGGCGTGAA GGACCCGAAA GACAAGGCCA GTCTCATGGG TGTGTGACCT 1260 GTGCGGTCAC ACAGAGCCCT GAGCTCAGCA GGGCCTGGCG CTTGATTTCA TGTTCTGTTG 1320 TCACCGTCTT GACATTCTTA TCATTTTTGA ACGAGGGGCC CTGTGTTTCC ATTTTGCACT 1380 GGGTCCCACA ACTGCTGGAG CTGGTCCTAC AGGAGGGTGA AAATTAGCAT ATAATGAGCA 1440 GTGAGGACAA CCAGGAGTCC CTTTCATTGC CATCTTGGCT TTGGTGGGCT TTGGCCAGCT 1500 TCTTTACCGC ATCTTATCAG TGGAGTCTTT GTGACCTGCA TCTTGTGAAG CCAGTCCTGC 1560 CCACCTCCTG TGTCACCCCC AGCTTAGAGA TCTGCATACA GTAAAATTAC TACTAGCTTT 1620 CTCCTGAGGC CCTGCAAGCT AAAGCTTATA CCTTGTGATA CAGGCGTGTC AGATTGCCAC 1680 CACTTTCCTG CTTTATAACT AAAGATGCTT TTGAGTCTAA TACCTGGATA GACTGTGTCC 1740 AGCATTAACC TTTTTTTCTT CTGTTCTCAT AAAAATCTCT CTTATTAAAA ATCTGTTTGG 1800 CTTTGTATTT CAGACAACAG AAGACTAGTT TTCCAGCCTA TTCACTTAGA TTCCAAATGG 1860 CATCTGATCT CTTATTTTTT TCTTTCTTAT TTTTTTAAAG AGACAAAGTC TATGTTGCCC 1920 GGGCTAGTCT CAAAAGCCTG AGCTCAAGTG ATCCTCCTGC CTTGGCCTCC CAAAGTGTTA 1980 AGATTACATG CATGAGCCAC CATGCTTGGC TTTGATCTCT TCTTTAAAAC TGGGCTTAAG 2040 TATTTTATGA ATTATCACTA GGTGCTATTT GATTTTAAAA ATATTTGTTA TATTCATCAG 2100 GTGTTCGGAC GGTTCAAGTT TATGTCTTCC AGGCTACAAC AGTTTCAGAG AAAAATAATT 2160 AGTCCAGTGT TCCAGCCTGT GCCACTGCAG AAAAGATGGA GTCCCTATAA GTCATTCGAT 2220 CAGGTACGAA GACATTTCTA TGCCTCCAGA GCAGGTAGGG ATGATGGCCC CTGTTCAGCA 2280 TGAAGCAGTG ACAGAAGATA GATCTCTGTC CTTCTACAAC CTCTTAAGAT TAAGGACGAG 2340 TATGTAATGT CTGAGGTGGG GATAAGATAG GAGGTTGGCA GGACTGGTTT CACAAAGACT 2400 CCTCGTATAA AACAGGATGT GGTAAAGAAG CCAAAACCCA TCAAACCAAG ATGGTGATGA 2460 AAGGGACCTC CGGTTGTCCT CGCTGCTCAT TATATGCTAA TTTTAATACA TTAGCATACT 2520 AAAAGACATT CCCACCAGCG CCATGACAGT TTACGAACGC CATGGCAGCA TCTGGAAGTT 2580 TCCCTAAGTA GTCTGAAAGG GGGAAGAACC TTCAGTTCCA GGAATTCCCA CCCCTTTCTC 2640 TGGAAAACTC ATGAATAATC CACTCCTTGT TTAGCACACG ATCAAGAAAT AACCACAAAA 2700 ATAGCCAACC AGCAGCCAGT CGGGACTGCT 2730
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