Tag | Content |
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EnhancerAtlas ID | HS108-41670 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr9:132348870-132351210 |
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) |
GSC | MA0648.1 | chr9:132350922-132350932 | GCTAATCCCC | + | 6.02 | ZNF263 | MA0528.1 | chr9:132349227-132349248 | CCCCCTCTTCCCTCCTCCCCA | - | 6.56 | ZNF263 | MA0528.1 | chr9:132349224-132349245 | TGCCCCCCTCTTCCCTCCTCC | - | 6.95 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34237 | chr9:132348280-132351519 | HCT-116 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I129586 | chr9 | 132348444 | 132350590 |
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Enhancer Sequence | AGACTTAGTC CAGCCCTCCA GGAAAGATGA GAAAACCAGC TGAGAAGCTG GGCCCAGGTG 60 GGTCAGGTCT CCTGTCTGCT GCCCCCAGGG GGAGCCCCCC ATCCGGCCTC CCCTCTCCCC 120 TCTGCCTGCT GAACCTGGCA GTGGAGTTGG GTAGGAGTGG GGGAGTGGGA GTTGGTGGTA 180 GGAGCTGCAG ATAGAATCCC CCAGGGAGGC AGAGGCGAGA ACGCTGAGCT CCTAGATCTC 240 CAGAAGAGCT ACAGCTGGCA GGGAAGGAGG CGGATGAAGC TCACATCTGG TTCCACCCAC 300 CCAGGCTGTG GCTCCAGTGG GCAGCACCGC CCTCCCTGCC CCAGGACTAA CCCCTGCCCC 360 CCTCTTCCCT CCTCCCCACA CTGTCTGCCT TCCTGGGGAG GCACAGCTGC AGATTTAGCC 420 GCAGATTCGT ATGTGTGCAT ACAGCCCAGT TGTAGGTGCT GTGTGCGCAT CAGAACACCA 480 ACTCCTGAGA GCTGACATTG AACCCCACCT TGAGACCTGA GGCCAATTTG CTATTATGTT 540 AAACGTACTG AGCCCCTGCT CACCCCGGAC AAATGGACGG CACCTGGGCC TCTCACCTCC 600 CAGGTGGAAT GGAGTTCCAG GTTTGATCTT GTTGGGATAG AAAGATTAAG GAAAGTGGCC 660 GGGCGCAGTG GCTCACACCT GTAATCCCAG CATACTGGGA GGCCAAGGCG GGTGGATCAC 720 TTGTCGAGAG TTTGAGACCA GCTTGGCCAA CATGGTGAAA CCCCATCTCT ACTAAATAGA 780 AAAAATTAGC TGGGTGTGGT GGCAGACACC TATAATCCCA GCTGCCAGGG AGGCTGAGGC 840 AGGAGAATCG CTTGAACCCG GGAGGCAGAG GTTGCAGTGA GTCCAGCCTG GGCAACAAGA 900 GTGAAACTCC GTCTCAAAAG AAAAAAAATA AGATAAAGGA AGGAAGAGGG GAGAAGACAG 960 CTGTACAGTG GAGATGGATT TATTGAGAGT AAACCTGAGA AGGGCTCTGG CCGGCATTAC 1020 AGCCTGAGGC TTTTTAAAGG GCCCGGTGGG GGAAGTGTGC TTTGAGAGAA GATCCTATTG 1080 GGAAGGAGTT GGGGAAGGGC TGGCTAGTTA TGACGAATGG GGACTTCGTT AGGCTCTGTT 1140 GCAGTTAGGG CCTATGCTCT GTTGAAGCTA TGGGCGGGGC TGACATTTGC GGACAGTTCT 1200 GAGACATGGA AATTTGATAC TTTAAGATGG TGGAGACCGG GCGCAGTGGC TCATGCCTGT 1260 AATCCCAGCG CTCTGGGAGA CCAAGGCGGG CGGACCACCT GAGGTCGGGA GTTCGAGACC 1320 CGCCTGACCA ACATGGAGAA ACCCCGTCTC TACTAAAAAT ACAAAATTAG CCGGGCATGG 1380 TGGCACTTGC CTGTAATCCC AGCTACTTGG GAGGCTGAGA CAGGAGAATC ACTTGACCCC 1440 GGGAGGCGGA GGTTGAGGTG AGCAGAGATT GCGCCACTGC ACTCTAGCCT GGGCAACAAG 1500 AGTGAAACTC TCTCTCAAAA AAAAAAAAAG AAGATTGTGG AGTCTCGTTA AGATGGCAGC 1560 ACTCTTGTCC TATCAATCCA GACTCTATGG TTAGATAGGG AGATGGGCTG GCGTGCTTTT 1620 TCTGGCTACT TCCTGCTGAA AGGGGGCCGT AAGATTGCTG GTTTTGGATT GACTGGAGGA 1680 GTAGCACCGT CTTCAGGTGT TGTTGGGGGG TAGTTTGTGA GATGGCTGTG ATCCTGTCGG 1740 TAAGGAACAT TTAACCAGGA ACTGATTTGG TTGGTTTTCT TGTCGCTCCC TCATTCTTTG 1800 AGCTCTTTCC TTAAGTTTTG GACGGCATCC CTTACCAAGC CTGGCTGGTT GAGATAGAAG 1860 CAGCATTCTT CCCCTAGAGA GAGGCAGGAA CCTCCCTTCT CTGTTGTAAG GAGGTCGAGT 1920 CCTCTCCGGT TTTGGAGGAC TCCTCCGGCT GGGGAGTCTA GCTGGTCTTG GATTCTTACA 1980 AGGCCCTTGG CTATATCTTC TGAGGATTCT TGTAGGTCTG TGGAGAGAGA CTTAAAATTT 2040 GAGAGTGAAG TGGCTAATCC CCCAGCTCTT AAACCAATGC CTGAGCTGAT GCCCAGAACA 2100 GCCTATAAGG CAATGATTTG GACTGCCCTT GTCTGTTTGA CATGCTGAAT GGAAGGCACC 2160 GGCAGGGCTG GGTTAGGGGG AATTATTCCG AAGCCTGGAG AAAGGGGGCC CAGAGTACAG 2220 GTGCCTGTCC AATCGGTTGG GAGGCAGAGG TAAGTGTTGG TGCCAGGCAG GAAAACAGGC 2280 CTGCTTCGGA AATGCAGGTA GAGATATGAA GGGAAAAAAG GTGGATTAAG GGCCTTTGGT 2340
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