Tag | Content |
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EnhancerAtlas ID | HS108-19904 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:17790350-17793000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ATF3 | MA0605.2 | chr19:17792494-17792506 | AATGACGTCACC | + | 6.07 | ATF3 | MA0605.2 | chr19:17792494-17792506 | AATGACGTCACC | - | 6.18 | EWSR1-FLI1 | MA0149.1 | chr19:17792149-17792167 | GGAAGGGAGGAAGCATAG | + | 6.42 | IRF1 | MA0050.2 | chr19:17791643-17791664 | CTTTTCTTTTTCTTTCTTTTC | + | 6.15 | JDP2(var.2) | MA0656.1 | chr19:17792494-17792506 | AATGACGTCACC | + | 6.44 | MEF2A | MA0052.3 | chr19:17791179-17791191 | GCTATTTATAGC | - | 6.32 | MEF2B | MA0660.1 | chr19:17791179-17791191 | GCTATTTATAGC | - | 7.22 | ONECUT3 | MA0757.1 | chr19:17792752-17792766 | ATCATTGATTTTTT | - | 6.07 | REST | MA0138.2 | chr19:17792561-17792582 | GGCGCTGTCCACGGTGCTGAA | - | 11.12 | SP2 | MA0516.2 | chr19:17791229-17791246 | AGGGGGGCGGGGATGAG | - | 6.23 | ZNF263 | MA0528.1 | chr19:17791470-17791491 | TCTCCTTTCTCCTCCTCTTCT | - | 6.22 | ZNF263 | MA0528.1 | chr19:17791480-17791501 | CCTCCTCTTCTTCCCTCCTCT | - | 6.29 | ZNF263 | MA0528.1 | chr19:17791473-17791494 | CCTTTCTCCTCCTCTTCTTCC | - | 6.31 | ZNF263 | MA0528.1 | chr19:17790515-17790536 | TGTCTCTCATCTCCCTCCTCC | - | 6.32 | ZNF263 | MA0528.1 | chr19:17791486-17791507 | CTTCTTCCCTCCTCTTCCTCC | - | 6.67 | ZNF263 | MA0528.1 | chr19:17791476-17791497 | TTCTCCTCCTCTTCTTCCCTC | - | 7.36 | ZNF263 | MA0528.1 | chr19:17791467-17791488 | CCCTCTCCTTTCTCCTCCTCT | - | 7.58 | ZNF263 | MA0528.1 | chr19:17791464-17791485 | CTTCCCTCTCCTTTCTCCTCC | - | 7.6 | ZNF263 | MA0528.1 | chr19:17791489-17791510 | CTTCCCTCCTCTTCCTCCCTC | - | 7.92 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_69003 | chr19:17790307-17791462 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 17791017 | 17791370 | chr19 | 17790400 | 17791527 | chr19 | 17792244 | 17792636 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I017679 | chr19 | 17790410 | 17791634 |
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Enhancer Sequence | GTGACAGGCT CTGGGGGGTG ATACAAGGGG CTCACTGGGG TCTAGACTGG GCTGGGCTCA 60 CTTGAAGCTC CTCCAACTGT GCCCTGTTTT ATAAACCATG GATTTAGGCT CAGCGGGGAG 120 CCCAGTAGCT CCTTGATCTG TTCTCTCTCT CTCTTTCCCA ATCCCTGTCT CTCATCTCCC 180 TCCTCCCCGT TCTATTTCTC TCCACTCTGG TCGTCTTCTT TTGGTCTCTG TTCTCTCCTT 240 CTCTCTCTCA CTGTCTCTGC CCTTCTTGTG CCCCTCCCTT GGTCAGTCCG GCTCCTCTTC 300 CCTAAGCCTC AGCTCCTTCC TGCAGCCTCT CTTGGCTAGA GGGGAATGGT CTCCGTTGGG 360 GTCCTCAGGC AGTGGGGGAC CGGCTGGAGG GCTGTACCCT CTGATAGCTG AAGCCAGGCT 420 CCTGCACTTA GCTCCCTGCC GAGGTCCAGG TTGAGGACAT CCATGATTTT TCATCACTGG 480 GGCTCCCAGT GGGAGAGGGG TCTCAGAGGG AAAAGGGGAC AGGAAAGGGG GCCGAGAGTG 540 GCGAGGGGGT TCTCAGGAGG GAAGGGTGTT CGCGGTGAGG GAGGGGATTC GGGAAGGGGG 600 ATGGGCGCAG AGGGGAGGGT GGTATCGGGG GAGAGGCTTG GAGGAGGAAG GGGGCTCAGA 660 GAAGGAACCC AGTCTCTCTC CCTGTCTTCC CCGGTCAGTA AATGGTCCCT GAGTCACCGT 720 CTTCGTCGTC ACATCCCGCC ACCTCCCCGC CTGCGCCGGG TTGCTGTATC AGGGTCAGCG 780 GGGCGGAAGC GCCACCCTTC CCCAGCGGGC TTCGGGTCAC ACGCATGAGG CTATTTATAG 840 CGTGGGCGCG CGGAGGGCGT GGGAGGCGCG CCGGCGGACA GGGGGGCGGG GATGAGGGGG 900 GTGCCCACTG CTGTCCCCAG CGACGAGCGG GTGAAGACAC CGCGTCATGC GGCCTCAAAG 960 GTCTTTGGGG CCCCCAGAAG CGCTGACTGA TGAATGTAGT GGCCGTACCC GGGGAGGCTG 1020 AGGCAGGAGT TCAGGCTGCG GGACACCCCT GCAGCCTGGC TTCGCGCCTC CGTTTCTGCA 1080 TCTGGAAAAT GGGGAGACGG AGTGGCTGAT CTCCCTTCCC TCTCCTTTCT CCTCCTCTTC 1140 TTCCCTCCTC TTCCTCCCTC ACCCCTTCTG CAGAATGATT ATAGTGTCAT TTATACTATT 1200 ATTATTATTA CTGATATCTT TACTGTTTTT ATTATTTGGT TGTGTTCTAA AGGTGTCCCT 1260 GGCCTGGATT CTAGGATTTG AATACCCTGG ATTCTTTTCT TTTTCTTTCT TTTCTCTTCT 1320 TCTTCTTCTT TTTTTTTCTT TTCTTTTCTT TTTTTTTTTT TTTTTTTTTT TGACAGGGTC 1380 TCTCTCTGTT GCCCAGGCTC CAGGCTGGAG GGCAGTGGTG TGATCATGGC TCACTGCAGC 1440 CTCGATCTCC CAGGTTCAAG CGATCCTCCC CACTCAGCCT CTCGAGTAGC TGAGACTGCA 1500 GGTGCGCATC ACCATGCTTG GCTATTCCTT TTTTTTTTTT TTTTTTTTTG TAGAGATGGG 1560 GTCTTGCTAT GTTGCTATGG CTGGCTTCAA GGCTCAAGCC ATCCCCTCGG CCTCCCAAAG 1620 TGTTGGAATT ACAGGCGTGA ACCACATGGC TGACTGACCC TGGATTCTAA TTAGGGGGGA 1680 CTGCAGTCTT GGGGCACTGG CTCCCTGACC TGCCACGTGG GATGGGGTGG GGAGACAGGA 1740 GGTGGAGATC CAGCCGTCTA GGGCTTCTGA AAGCCCACCC GCCCCAGGAT TAGCTTGGGG 1800 GAAGGGAGGA AGCATAGAGA ATCCAGAAAT AGATTATAGG AGATTTGATC GTTTTGTGTG 1860 TGATGTTGGT GGAGGGCATT TCAGCGGGAG ATGGATGGGC TTTAGGATAA AAGACCTCAG 1920 CTGTGCTGGT TTCGCATCTG GGAGACACTA AATGAGGACC CTTATCCTCC GTTGACACAA 1980 ATAGACCAGA GCCAGACTGA GCCTTCAGTG TAAAAAACAC CAAGAACCTG GAGTTCCAGA 2040 GAGCTTCGGG AATAAGGGAT TTGTGTGTGT GTTGTTTACC ATGAACCACT TAGAAGTAGG 2100 CCTAGCCTAT AGTAGGTGCT CATTAAATAG TAATTCACGG AAGGAATGAC GTCACCTCCT 2160 CCATTAATCC TGGGAGGCTG AGCTAAGAGC TGTCCCCCAG AGGCGCGGGC AGGCGCTGTC 2220 CACGGTGCTG AATGCTCGGT CCCACCCGTG TACCCTCAAC GAACTAGGCT CCCTCCTGGA 2280 GTGGCCCTGG GGGACCCCTC TTGGAGCGCT CCTCGGGCCC CAGAATGCAG TGGACTCTCA 2340 GAAATGTCCT GCACTCAGAA CCGCCTTCCA GAAAGCTTTT AGTCTCCATT AATAAAAACA 2400 TCATCATTGA TTTTTTTTTT TTTTTTTTTT TGACGGAGTC TCACTCTGTA GCCCAAGCTG 2460 GAGTGCAGTG GCGCGACCTC GGCTCACTGC AACCTCCGCC TTCGGGGCTT AAGCGATTCT 2520 CGTGCCTCAG CCCCCTGAGT AGCTGGGACT ACAGGCGCGC GCCACCATAC CCAGCTAATT 2580 TTTTTGTATT TTAGTAAAGA CAGGGTTTCA CCATGTTGCC CAGGGTGGTC TTGAACTCCT 2640 GAGCTCAGGA 2650
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