Tag | Content |
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EnhancerAtlas ID | HS108-18153 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:81059940-81062770 |
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) |
KLF5 | MA0599.1 | chr17:81060350-81060360 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr17:81060382-81060392 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr17:81060413-81060423 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr17:81060477-81060487 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr17:81060509-81060519 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr17:81060541-81060551 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr17:81060571-81060581 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr17:81060602-81060612 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr17:81060697-81060707 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr17:81060728-81060738 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr17:81060759-81060769 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr17:81060791-81060801 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr17:81060823-81060833 | GCCCCGCCCC | + | 6.02 | PLAG1 | MA0163.1 | chr17:81061314-81061328 | GAGGCCAAGGGGGG | + | 6.06 |
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| Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
SE_01998 | chr17:81058746-81060371 | Aorta | SE_01998 | chr17:81060848-81063603 | Aorta | SE_23159 | chr17:81058726-81060419 | Colon_Crypt_1 | SE_24692 | chr17:81058755-81061266 | Colon_Crypt_3 | SE_24692 | chr17:81061731-81062425 | Colon_Crypt_3 | SE_26841 | chr17:81058765-81061145 | Esophagus | SE_27794 | chr17:81059812-81060477 | Fetal_Intestine | SE_32097 | chr17:81058901-81060299 | Gastric | SE_35080 | chr17:81058816-81061950 | HeLa | SE_43234 | chr17:81058821-81060455 | Lung | SE_43234 | chr17:81060691-81062567 | Lung | SE_44287 | chr17:81058879-81060315 | NHDF-Ad | SE_44287 | chr17:81062120-81064768 | NHDF-Ad | SE_50617 | chr17:81058789-81060926 | Sigmoid_Colon | SE_52664 | chr17:81059172-81060261 | Small_Intestine |
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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 | TTGCCCCAGC GATCAGGCGC CTGAGCTTCC TCCCCCGAGC CTGAGTCCAG CTGAGCTCCG 60 TGTGGCTTTC CCGGTGGAGC AGACTCTGTC TGATTTCCCG ACGGCTGGCG CCTCCACCTG 120 CTTCCCAAAA CCGAGCACCA GGGGTCTGAG AGGTTGCTAT GGGAAGGTCG CTTGCTCCAG 180 GGGGCCCTGG AACAGTTGCT AAGTTTAACG CCCTGGCCCA GGATCCACCT GTCCTGCTGC 240 AGACCAGCCC TGCTCATTCC TCCCTCTGGC TGTGAAGATG GAAGCCCATG GGTTGGATGC 300 CTCGGGCCAG GGCTGTCACG CAAGGAAGCC TGGGGAGGAC TGTGGCACTG ACCCCATGGG 360 CCATGGTATC GCCTCAGGGC CCTGCCCCTC TGGATCTCCG TCTCCTCAGG GCCCCGCCCC 420 TCTGGATCTC CGTCTCCTCG GCGCCCCGCC CCTCTGGATC TCGTCTCCTC GGCGCCCCGC 480 CCCTCTGGAT CCCTGTCTCC TCGGGGCCCC ACCCCTCTGG ATCTCCGTCT CCTCGGCGCC 540 CCGCCCCTCT GGATCTCCGT CTCCTCGGCG CCCCGCCCCT CTGGATCCCC GTCTCCTCGG 600 CGCCCCGCCC CTCTGATCTC CTCTCCTCGG GGCCCCGCCC CTCTGATTCC AGTCTCCTCG 660 GCGCCCCGCC CCTCTGGATC TCCGTCTCCT CGGCGCCCCA CCCCTCTGAT CTCGGTCTCC 720 TCGGCGCCCC ACCCCTCTGG AGTTCCGTCT CCTCGGGGCC CCGCCCCTCT GGATCTCGTC 780 TCCTCGGCGC CCCGCCCCTC TGATCTCGGT CTCCTCGGCG CCCCGCCCCT CTGGATCCCC 840 GTCTCCTCGG CGCCCCGCCC CTCTGGATCT CCGTCTCCTC GGGGCCCCGC CCCTCTGGAT 900 CTCCGTCTCC TCGGGGCTCC GCCCCTCTGA TCTCCTGCAC GCACCCGGCC TCGCCTGAAA 960 AGCCCCACGT ACAGCAAAGC GGCCGTGTCT TGGTGGCCTC TGCCTGGGGC GCTATGGGTG 1020 GCCTGTCTAT GCCTCAGTTT CCCCATTCTT GATGAGAGGG AGCTGGGGTC GCTACTGGTC 1080 ACTCGGGCCC CAGGCAGACC AAGGCTCACT TCTGTCCACT CCCTGGCCCC ATTCCCAGGA 1140 ATCCCACCGG TTCCTGGCCG GGGTCTGGAA TCTGTTCTCC CAGTCCAGGA CCTACCCTCC 1200 CCTCCACTTC CTGCCTGCAA GCTCTGTGGT CCTTCCTTGT CTTGAGTCCA GGGTTCCCTG 1260 TGCTCCCAGT CCAGCCTCCC TACTCAGGGC CGAGGGCACC AGGAGGATGG TCGTTGCAAA 1320 AGAATATGGG AGGCCGGGTG CGGCGGCTCA CGCCTGTAAT CCCAGTACTT CTGGGAGGCC 1380 AAGGGGGGCG GATGACTTGA GGCCGTGCAA CACCTGCCAG CACCAGCATT TGACACGGAA 1440 TCGAAGAAAA CAGGCAGGAC ATACCCTGAC TACACTAGTA CAAGTCATCG GCGTCTCGGG 1500 GTCCTGGGTT TTAGAAATCA CACTGTCAGG GAGGGCTGAT GGGGTCCTGG GTTGGAGGCT 1560 GGAAGTGGAG GAATCGAGGC ATAGGCAGAA ACTTGAAGGA AGGGTCAGCC GAGCTGGCCA 1620 GAAGGGGGCT CCTCGCCACG GTCCCCAGGG AAGCACTTTG CTCATGGGCC CCGGCCCTGA 1680 GAGAGGAGCT CCTGCCTCTT CCCACTCGGA GAGGGCTGAC AGGAGAGGCT TGGCCTGGTG 1740 TTTCCTGATG AGATAGCGGG CACGTTCCGG GAAGCGGTGA GCAGGCCCAG CAGACATCAG 1800 ATGTGGTGCT TCCTGTCTCC TGTGAATGCG CCTGGCCCTT GAGGGGGGTC TGGGATGGAG 1860 AGTCGGGGGA GGGGAACCCC ACTCGCCCTT CTCCTTGTTG TTCTTGGCAG CTGGACTTGG 1920 GCAATTGTGC CTCCACCCTC TGGAGGGGCC TCCCCCTGTG CTGGCTGCAG ATCAGAGGGG 1980 CGATGGGGAG GGATCCACCG GTCCAGGCGG GGGCTCACCT TCCAGACCCG GGCGTGGGCG 2040 AGAGGGGTGC ATGGGAGGAC GCCCGATGCC TCAGGGCCCC CGGTCAGCAG CGAGGCACAG 2100 ACTCTCCTCT GGGCGGTGAT GGCCCTGCAC GAGGTCCGTG TGCCGTCTGC CTGCACAGGG 2160 AGAGGAAAGG ATCACGCGAC CATGGGTACG TTGGCCACCT GAAGGTTGAG TCCCGCAGCC 2220 TAGAGACTGG AGCGTGGGGA CCAGGAGGAG CTTCTTAGCG GAACTGGGCT GGGGCTCATG 2280 CAGCCCTCCA GGAGCCCCCG ACGCGACGCC CTGGCTCATC CCGGGTGAAG AGGCTGCTGA 2340 GTCTGAACTG ATGACAGTGG ACGGGTGGCC GCCGGTTCCC AACGCATGGT TGGGCCTGGA 2400 ACCCAGGTGA CTCTGGGAGA TGTGGTCACA GTCACAGCCG TCTGTGGGCC TTTGGGTTCA 2460 AAACAGCGCG AGTCACAGGA GACAGAAGGG AATCTGAGCT TGCGATTGCT CATTCTTGTC 2520 ACCCTCCTGG CTCTGGGACA CCTCTGCCAT CTCCTACCAA GGGTACCCCA TTCCTGGCGA 2580 GTTGGAAAGT GGCCTCATGG GCAGAAAACG AGGGCAAAGG GAGCTGCGTG CTGTGAGAGA 2640 CGTCCCCGCA CCCACCCTCC CCACCAGCTC CCTTGGGCCT TTCCTCCCTC CCAGCCCCAC 2700 CCACAGCCGG GTGGCTCCCT TCACTGTCTC TCCTGGGTTT AACTCAGAGG CTGGCGAGCA 2760 GGGGCTGACC AGTGTGTGTC GGAGACTCTC CGAGTGGCCA GCACGGGCAG GGAGCTCATA 2820 GGCTTGGCCC 2830
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