Tag | Content |
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EnhancerAtlas ID | HS108-09588 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr12:53266420-53269690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr12:53268149-53268160 | GGTGACTCATC | + | 6.32 | GLIS2 | MA0736.1 | chr12:53267812-53267826 | CACCCCCCGCAGAG | + | 6.27 | JUND | MA0491.1 | chr12:53268149-53268160 | GGTGACTCATC | + | 6.62 | KLF5 | MA0599.1 | chr12:53268041-53268051 | GGGGCGGGGC | - | 6.02 | Nfe2l2 | MA0150.2 | chr12:53268231-53268246 | GAGCCTGACTCAGCA | + | 6 | RREB1 | MA0073.1 | chr12:53266718-53266738 | CCTCCCACCAACCACAACCA | + | 6.34 | RREB1 | MA0073.1 | chr12:53266722-53266742 | CCACCAACCACAACCACCCT | + | 6.46 | RREB1 | MA0073.1 | chr12:53267483-53267503 | TGTGTGTGTGTGTTTTGTGG | - | 7.29 |
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| Number of super-enhancer constituents: 18 | ID | Coordinate | Tissue/cell |
SE_23067 | chr12:53263490-53272120 | Colon_Crypt_1 | SE_23945 | chr12:53263966-53269591 | Colon_Crypt_2 | SE_26564 | chr12:53260695-53274096 | Esophagus | SE_27647 | chr12:53266844-53268884 | Fetal_Intestine | SE_28539 | chr12:53266210-53268837 | Fetal_Intestine_Large | SE_34862 | chr12:53263401-53270367 | HeLa | SE_43420 | chr12:53263602-53268189 | MCF-7 | SE_43420 | chr12:53268221-53272157 | MCF-7 | SE_47304 | chr12:53268049-53268943 | Panc1 | SE_47563 | chr12:53267361-53268127 | Pancreas | SE_47563 | chr12:53268138-53268548 | Pancreas | SE_52377 | chr12:53263981-53269471 | Small_Intestine | SE_56286 | chr12:53264201-53266907 | u87 | SE_56286 | chr12:53266989-53269158 | u87 | SE_57699 | chr12:53267231-53268954 | VACO_503 | SE_64566 | chr12:53266900-53273597 | NHEK | SE_65517 | chr12:53267217-53269253 | Pancreatic_islets | SE_67099 | chr12:53263476-53274484 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 6 | Chromosome | Start | End |
chr12 | 53268845 | 53268952 | chr12 | 53269132 | 53269285 | chr12 | 53269339 | 53269484 | chr12 | 53266499 | 53266553 | chr12 | 53266726 | 53268796 | chr12 | 53267781 | 53268340 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I052869 | chr12 | 53263583 | 53270635 |
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Enhancer Sequence | TGCCAGGGTC AGGAGCAGGG ATGCCTTCTA GCTCTCCCTG GCTCTAGAGC ACCATTTCCA 60 AATGCCCCCA GCTCCAGGAA GGAGTTCAGG CAAGAGCTGG GGAGCTGCAC AAGGCAAAGT 120 AGAGCAGAGC TGCCTAAAAC TGTCCAGGGC CCAGAGGGCC ATTCCCAGGG GCTGGCGGTC 180 CCCCTCGGGC TACTTCCCAG GCCAAGCAGC CAAATCCCCA AAACCGGAAT CCACCAACCC 240 AGAGGACCAC CGCCCCTGCT GACCGCCAAA CCGTCCCTGG AGAACCAGAC CATTGTGCCC 300 TCCCACCAAC CACAACCACC CTGGGGGCCC CCACCCTGGA GCTCATGCTG TTGGGAGAGG 360 GTAGGGCCTG ATTTCAGGTG ACAGTGGAGA AAGGATGGGG TGACTGCTCT TGGGGACAGA 420 GAGTGGCGTG TTGGAAGAAT GAAGGCGTCC TGTCCCTGGG GCTGAGTGGG AACCTGAGCA 480 GGGCAGGCAC CGCCCGACGC GGAGGCCTCC ACCCCCAACC CAGCTGGGCT GCCTGCTCCC 540 ATCACACCCT GGGCAGTAAA ACTTGCTTTT ATGGTTGTTG CGGGGGTTGT TTTCCTTGGT 600 GGTGGGGGCA GGGGGTTCTG TTTGTGTCTT TGTATCTTTG TGCAAATACA CCTGTGTTGA 660 TATGTGCCTG CTCCTATACA TGTATTGATG TCTGAGGTTT TGTGTGTGTG TAAATCTGCA 720 TGTGTCCATG CCTCTGTGTG TGGATATATC TGTGGGGGAG ATCATCATAG CTACCATTTA 780 TTATTTCAAT GTACTCTCCA GGTGTTGTTT CCTTTAATCC TCGGACAATC CTTTAAGGAA 840 GATATTCTAG CTATCCCCAT TTTACAGATA GGGCCATAAG GTTGGAGAGA TCCGATAATT 900 GACCCAAAGT CAGATCACCA GTAAGAGGCA GAACCAGGAG ACTTCCCTCT ACTGCTGAAT 960 GTGTCTCTCT GTGTGCCCGA AAATAAAGAG CTATATATGA GAATCGTGTA ACATCTGTCT 1020 GTGTGTGTGT CTGCACCGTC TAAACCTGTG CATGTGTGTG GGGTGTGTGT GTGTGTTTTG 1080 TGGCCCAGGT GCAAGTCAGG TGCACCTGCC AGCAGCTGGC ATCACCAAGG TCTTAGGGAC 1140 AGTGGCCCTC TGAGCATATT TTCTGACTGT ATTGTCCCTA GAACAATTTC TGAAGCAGAT 1200 GACAGCGTGT GGTGTTGCTG ACTGTGGACA GAGAACTTCT GCCGTCAAGA CCGTAGCAGG 1260 AAATGCCCCT GTGCCCCTGA GCCTGGCAAA CAAGGCAGCC TGTCTCCTTC AAGGAGGAGC 1320 TGAGTGCCCC GCAGAGACAT TCCGGGAAGA GCTCAGAGGG GGGTAAGAAG GAAGAAGAGC 1380 GAGGCTGCCT CCCACCCCCC GCAGAGCCAC CCGTGCCCCT AATCCACAGG TGGGAGTGGC 1440 GGGGAGTGGC CCCTCGAAGA GGAGCTGAGA CGTCTCCGCT CGGTTCCCCT GAGAGCCCTG 1500 TGCTCCGTCA CCGACAGCCT CTCTCCAGAA GTAGAGACCA TGGAGTCTGG CTGGGTGCCG 1560 CGTCAGGGGT CTCTCGGGGC GGCTAGAGGC CCTGGGAACC TGGAAGCCCG CGGGGCGCGG 1620 CGGGGCGGGG CAGAGCGCTA GAGCCGGGTG GCGGCCGCCG ATTGGCTGGG CCCGAGCGCT 1680 CCCACGGCGG CCGGGGGCCC CAGGGCGGCG CCGGCCGCGC CCGCTCCGCG GTGACTCATC 1740 CAGCACCCCA CCTCTGGAGC TGGACGGGCG CCCGGCCTCT TCCCACCCCA GACCCGCCCG 1800 CTAAGCCGGG AGAGCCTGAC TCAGCAGGGG GAGCCTGGCC TGCCTTCCGC CCCCTTCGCG 1860 TCCTCCCCCG GGGCAGAGGA GAGTGTTGTG GGGAGAATGC GTTTCTGTCC CTGTGGGAGA 1920 ATTTGTCCCG CTCTAGGGAG GAGAATCTGG TATCTGTTCT TCTGGGAGAC TGTGTGTCTG 1980 TCCATGGGCG GTGGGGCCTT CTGTCCCCAC AACGGGAGGT TGTGTGCCTG TCTTTCTGGG 2040 GGTGTCTCTG TGTCTTAAGA TCTTTATGAG TGTGGCCGAT GGACTGTGGT CTTTTGGAAT 2100 CTGCCTGTTG GTCTCTTTGG AGCATCACTG ACCTCCACCA CTCCAGATCA TCTCTGTGCC 2160 CCCCTACACC CCACTTCCCC AGAAGTGGGG AAGAGCTTAG CAGCTCTGTG CCTCTGTCTC 2220 ACAGCGGCCA GGACAGGCCC CTCAGGGGTT AGCTCTGAGT AATTCTCCAG CTCTGGCTCT 2280 GCCCCCTCCA CAGTGCCAGG GCCCCTGAAG GTCTGGGGCC AGATGCTACC CTGCAGGCCA 2340 GGCTCAATCC CTACAGCAGT GCCTGAAATA TCTCAAAGTG ATTTTAAAGC AAGATCTCAA 2400 AAGTGATCTT AAACCAAGTG ATCCCTCAAA AAGGGAAAAG GACCCACAAT TGTCCAGAGA 2460 CTACTGTGGG CCATGTGTGC CATGCTAGGA GCTTCGTGTT CACCTTATCG ATGCTTCTCA 2520 CAGCAACTCC AAAAACAAAC ATAATCCCCA TTTTACCGGG GAGAAACTGA GGCCTACGTG 2580 GTGGCTCAAG GTCACACTGG CACAGTATAT GAGCAAATCT GGATTTGAAC CCAGGACTCT 2640 CTGGCTCTAA AGTGTATGCT CTTTCCACGG CTGTGGCTGT TCCCTGAGCG CCTTAGCCAG 2700 GAGTGGCCTC CACCTGGCCC CACAGCAAAC CTGGGGGAAA CTCCACCACC TCCACAGGGA 2760 GACCAGCCTT CAACTTCATC CAGGCTTTCC CATACCAAGA GAGGATCCCC CAGGACTGTG 2820 AGAGGGACTG GGGTGGGAAG GAGAAAGAAG CCAAGAGTCA GTACATGTGG GGTTTGGAGT 2880 AGGCAACAGG ATATGCCAGA TCCCGGGGCT GGGGAAGAGG ACCCTGCAGC TCGACCCACG 2940 CACACTTTGT AGGACACACA CACACACTCA CATACACATG CACAATGGCT GCTGGACACA 3000 GTGCACAGAT CCAGCTGTGG GGGTCATTGC AAAGATGCCC AGACACACAC ACGTGCATGT 3060 TTCATGTGGT GCACACCTGA TATATAGAGC TGTTACCAAC AGACATGAAG GAATCAGTGG 3120 AGTCATTACA CACAGATTCA CAATGGTGTG CAGGTCATTA CTCACACACA CACACACACA 3180 CACACACACA CACACACACA CACAGTCAGA ACCACCAAAA AGAGGATGAT GAGGGAGTGA 3240 GAAGAACGTT TGAAGCTGTT GTAGGAACAA 3270
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