Tag | Content |
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EnhancerAtlas ID | HS111-03212 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr20:60932400-60935380 |
Target genes | Number: 13 | Name | Ensembl ID |
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SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr20:60934294-60934305 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr20:60934294-60934304 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr20:60935113-60935123 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr20:60932553-60932563 | GGGGCGGGGC | - | 6.02 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_01180 | chr20:60929978-60935127 | Adrenal_Gland | SE_01814 | chr20:60926311-60935381 | Aorta | SE_02986 | chr20:60930057-60933506 | Bladder | SE_02986 | chr20:60933595-60935141 | Bladder | SE_06600 | chr20:60929269-60935458 | Brain_Hippocampus_Middle | SE_26675 | chr20:60924634-60948281 | Esophagus | SE_32162 | chr20:60929761-60935428 | Gastric | SE_32788 | chr20:60933260-60933835 | H1 | SE_32788 | chr20:60933855-60935060 | H1 | SE_34294 | chr20:60929439-60935428 | HCT-116 | SE_34663 | chr20:60929440-60946757 | HeLa | SE_40786 | chr20:60926918-60935399 | Left_Ventricle | SE_41611 | chr20:60924954-60935371 | LNCaP | SE_42250 | chr20:60924752-60935423 | Lung | SE_47289 | chr20:60927618-60935422 | Panc1 | SE_47683 | chr20:60933015-60934488 | Pancreas | SE_48780 | chr20:60929111-60935392 | Right_Atrium | SE_49542 | chr20:60929925-60934554 | Right_Ventricle | SE_54169 | chr20:60930141-60935515 | Spleen | SE_54617 | chr20:60926003-60935405 | Stomach_Smooth_Muscle | SE_56802 | chr20:60931526-60935523 | VACO_400 | SE_57434 | chr20:60926913-60935529 | VACO_503 | SE_57942 | chr20:60932744-60935423 | VACO_9m | SE_61548 | chr20:60911909-60958488 | Toledo | SE_65356 | chr20:60926919-60942327 | Pancreatic_islets | SE_68688 | chr20:60927598-60935475 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 60934158 | 60935163 | chr20 | 60934143 | 60934390 |
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Enhancer Sequence | GCCAGCACCC TGATCGCACT GCTCGGACAG GGCACCGGGG CACCCAGCCC CCTCGATGCC 60 CAGAGTCCTG GGCCAGCCCA GCCCTTGCCC GCTCCTGCTG TGTGCCTCCC CTCGAAGAGA 120 CCCCATCTGG AAACGTAGAT AAGCCCCACA GCAGGGGCGG GGCGGCAGCC GGGAGCATCT 180 CCACTGGCCC CCAGCTGGGT GAATAAGCAC GGCGGCCACA CAACCTATCA GGGGTCCGGA 240 AACGTGCCCC ACACAGACAC CTCTCCCAGA GGGACGTGGA GTGGAAAAGC CGGGGGTTTC 300 CACAGCAAGC CCACCGCTGG GAAGAAAAAT AACAACTCTG AGGCCAGAAC CCCCAACTCT 360 GGGGTTGGAC GCCGCCATGC CCAACTACAG ATGTCCTAAG CAGGACAGGA AAACTTCCAG 420 GAGTGGGCGG GGGGACAGGA GCTCCCCAGC TGGAGGGAGA GGATGGGTTC CCAGCCAGGG 480 GGCTGCCCGC ACCTCAACAG AGCTGGGCCT GGGGTGGATT CAGGGACCCC AACCACTGCA 540 GCCCAAGCTC CAGGCTCCCT CCCTGCAGCC CAGCCCAGGT CAGGCCAGAT GGTCAGCCGG 600 GGACACAGGA AGTGGAGATT ATCCCAAGGG GACCCCTCGG CCTGAAACCC AAACAGTTTC 660 GTCTTCACTG AGCTGTGTTG TCAGAGGCCA ATGTGGTGGC TCTTGTTTAG AAACAGACAG 720 AAAACAGGAA GCCTTTGGGG ACCACCAGGG CCTGGGGGGT CTAGGTGGGT GCTGGGGCAT 780 CTCTGTGCCC TGAGTGCCAG GTCTGGCCGT GCAGCCACCA AGGGCAAGCA TGGCGCGGGG 840 GTGCGGGGAG AGGAGCGGCC CCATCCCCAC CTTGGCATGG CAGCCCCTTG GGCCGTGTCC 900 TCCTTCCAGG ACACGTAGAG GGAGGGTTTT GCCGTCTATC CTGTGCCAGG GGAGGGGAGT 960 GGTGCCTCCC AGGACCCCCG CCGTACCCCC CAGGGAGCCC TGCTCAAGTG GCTGCGTCTG 1020 GTTCAGCCCG TGCACCTGTC CCGGCCGCCG AGCTCTGTAA CTAGAGCCTG GCCGCAGCTG 1080 CACTTCCTGT CCTTCCCTGG ACAACCCACT GACCGTCCTG GGGCACTGGC CACATGGCTG 1140 AGTGCCCAAC CAGGCCCAGG GAGCCAAGCC AGTGGCACCC TGGACCAGTA GGCCTGCCCA 1200 GGGCCCAAGC CGGCCAGCCA GAGAGCAGGC AGTCCTGAAG GGTGAGGCAG CCTGGGCGCG 1260 CTGGGCCTCC GGCAGGTCCT CCTCCTGCGG TGCTCCTCCC ATTTACAGAG GAGGAACCAG 1320 CCCGGGAACC CAGACTGCAG ACAGCATGGC CAACCCCACA GTCCTCCAGA CCCCAGCACT 1380 GGGACCTTGG GCACTCCACA CTGGCCCTGA CCCTCTCATA ACCCCACCTC AGTTTCCCCA 1440 AGTGCCTAGG GAAACTCACA CTCCAGTGGC CAATGACTTC AGCAGAGCTT TGCCTCCTTG 1500 TACCCCCACT TGGAGGGGAC AGCTGACTGC CTCCCCTCTC CGGCCCTACC TGTCCACTCT 1560 GCCCTCCCAT GGGTCTCCAC CATCCCCAGG GGCACAGGCC CTCACCTGGC ACTGCTCGCC 1620 CCCAACCAAT ACTTCTAGCC TCATGCCTAA CTGCCCCCTT ATACCCTGCC AGCCCCAGTT 1680 CCCCCACACC TTGACCCCCA CCTGGGCCTC CCCATTTGCC CTGCAGCTCT GGGCCTCGGG 1740 GACTGGGACA AAGCCGCTAC CCCACCTGTA GCACCTGCAG CGTGGCCTGC TCTACAGAGA 1800 ACAAAGCAGG GGCCTCCCTA CCGGAAGGGG GCCCGTGCGT CCTCACTCCT CATCTGAGGG 1860 AGGCGGGAGG CAATGCCCTC CTCTGCTGGG GAGAGCCCCG CCCCCACGGT CAGGCCACCC 1920 AGGGGCCGAC TGGAGAGGGA GGGGACACAG GCCAGAGCCA GCCCCACTCA CCCTGCCCAG 1980 CTCCTTACAA CCTGGGCCCG CTGGGCTAGC GTGCTGGTGT AGTGGGGCAA GGGCCTGGAC 2040 CCTGCGGCAG AGCCAGGGGG TGGGGGAGCT CAAGCCAGGA CCCGCTGGCC ATGTGCCTGG 2100 GCAGTCATGA ACGCGCTCAC CCTTCCCTGG GCCTGGGGCC TGGGGCCTGG GGCCTGGGTG 2160 TGGTTCTCGG AAGAAGGAGC CTGAGGCCAG TGATGTGGCC GCTCAGTTCC AGAAGCTTCC 2220 GGAGGATGCA AGGAGATACG CAAGAACCCC CTAGAAGGAC CCCCTGGGGA AGGTCACGTC 2280 TGGAACTCGG AAACTGCCCC CTGAGTCACC AGTGACCAGC GCTGGAGCCT CTTCCTGAGG 2340 CCCCACCCTT GGAGAGAGAA CCCCTCCACG GCTGGGCGCA GCGGGACCCA GGCCAGGAGC 2400 CCAGCTGGCA CTCCCGGGGG CCCAGGCTCA GCTGCTTCTG GGTGGACACC ACAGGGACTA 2460 GTCTCCCCTC CCCTGCGCCA GCCCCTGCCC CACCGCACAC CAGGGGTATG AGATCCGAAC 2520 CGTGATGCAG CCCACCCCGC CCTCCTCAGC CTTCCAGGAG CAGGAAGCCT TCCCGATGCC 2580 CAGTGCCAGC CGCCCCCACC CCCGTCCCAG GGCATCCGCT CCAGATCCCA GAACAAAGGC 2640 TGCTGGCAGC CCGCTGCAGG GGGAGTGCCC GGACCCACCC GCCGCTCAGC CTGGCTTCCT 2700 GATGGAGGCC CCAGCCCCGC CCCAGGATCA GCCCTGAAGC CCAGGAAGGA CATTTCCCCA 2760 CCCCACTCCA GGGAGTCCCT GCCCCCACCC TGACCAAGGC TGGCAGCCCC CTGGCCTAGG 2820 CCGAGACAGG GGCCTTGGTA GATACATCCA CGTGGTCAGG AAAGTGGGTG AGAAGGAAGG 2880 AAGACGGTGC AGGTGTGGAG GGAGGAATGA GCAGACAGGT GGACAGATGG ATGGAAACAA 2940 GGAATAAAGG GTGGGTGCTG CATAGGTAGG GGGGTGGGTG 2980
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