Tag | Content |
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EnhancerAtlas ID | HS111-02144 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr17:27071270-27074230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:27073965-27073984 | AGCTGCCACCTGTTGGCCA | - | 6.22 | Gfi1b | MA0483.1 | chr17:27072276-27072287 | AAATCTCAGCA | + | 6.32 | KLF16 | MA0741.1 | chr17:27071299-27071310 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr17:27071300-27071310 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr17:27071305-27071315 | GGGGCGGGGC | - | 6.02 | NFIC | MA0161.2 | chr17:27073787-27073798 | TTCTTGGCAGA | + | 6.02 | NR2C2 | MA0504.1 | chr17:27073772-27073787 | TGACCTTTGCCCTGG | - | 6.54 | Nr2f6 | MA0677.1 | chr17:27073772-27073786 | TGACCTTTGCCCTG | - | 6.45 | REL | MA0101.1 | chr17:27072594-27072604 | GGAAATCCCC | - | 6.02 | Rxra | MA0512.2 | chr17:27073772-27073786 | TGACCTTTGCCCTG | - | 6.09 | Sox3 | MA0514.1 | chr17:27072290-27072300 | CCTTTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr17:27074202-27074223 | CCTTTTTCCTGCCCCTCCCCC | - | 6.55 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_05632 | chr17:27069997-27078317 | Brain_Cingulate_Gyrus | SE_08725 | chr17:27071068-27078352 | Brain_Inferior_Temporal_Lobe | SE_10640 | chr17:27067172-27073896 | CD19_Primary | SE_11107 | chr17:27063941-27074852 | CD20 | SE_23379 | chr17:27069458-27077129 | Colon_Crypt_1 | SE_24020 | chr17:27070110-27075174 | Colon_Crypt_2 | SE_24922 | chr17:27069971-27076880 | Colon_Crypt_3 | SE_27507 | chr17:27069942-27077307 | Esophagus | SE_28448 | chr17:27069282-27074805 | Fetal_Intestine | SE_31712 | chr17:27069439-27077924 | Gastric | SE_41613 | chr17:27070124-27077046 | LNCaP | SE_48035 | chr17:27070973-27075260 | Pancreas | SE_50731 | chr17:27067846-27077893 | Sigmoid_Colon | SE_52894 | chr17:27069443-27077918 | Small_Intestine | SE_56907 | chr17:27069989-27075247 | VACO_400 | SE_57743 | chr17:27070072-27074688 | VACO_503 | SE_58111 | chr17:27070084-27074792 | VACO_9m | SE_59037 | chr17:27064076-27076014 | Ly3 | SE_60572 | chr17:27064057-27078318 | DHL6 | SE_61391 | chr17:27064119-27074342 | HBL1 | SE_65750 | chr17:27067329-27077753 | Pancreatic_islets | SE_68764 | chr17:27068899-27078085 | H9 |
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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 | CAGGTGCTGG CCGGGGAGCA GGGGACAGCG GGGGCGGGGC GGGGCGGGGG GCGCCGCCTG 60 GGGAGGGTCT CGGGCCCGGG GCAAGGCGGG CCTTTGTCTG CGCTGCGACC CTGTGACCTC 120 AGGGGCGCCC CGTGACGTCA CGGGGAGGGA TGACGTCAAG CCCCGAGGGA GGCCCCCCCC 180 GCAGGAATCC GAGGGGTCCG GGCGGGTCCC AACTGCCCGG CCCGGGGCGG AAGACCTCGG 240 CGCCTTCTCG TGGGGTCAGG AGGGGAAGAG GCCCTTCCCC GTCACCTGAG AGCCGGCGCG 300 GCCTCAGCCT TGAACTTTGA ATCCTGGGGG AAGAGGACAA AACCCGCTCC CGCGTGGCAG 360 TTTGAGCCTC CGGAGCTTTC CCCCATCTAA CCTCTTCTGA TTCTTCGAAC GTTCAGAGAA 420 CGGTAGCTAT TGTTCTCCCA TTTCACAGAT CATGAAACGA GATTCAAAGA AAGGCTGCGA 480 CTTGCCCAGG GTCACATAGT TACTTAAAGG CTTAACTAGG ATTTAAACCC GGACTGCTTA 540 TGATCACACA ATGGAGGAAG GACTGAATCC TCCCCCGAAG AAGGACCCCT CTAGGCGGCT 600 CCCCTCTCTC CCGGGGGCTG GAGTAAGGCG GGTGGTCCAT AAGTCATGAA GAAGGGGGTC 660 GCACTCGTGT TGTTACTGAA CTCCCGCTGC CCTCTCAGGA CGCAGGTTAG CCCTTGGCTC 720 TTGGGCATCC ATCAAGTTTC TGGGCGCCCT GTATGTCTTG AATCTCCTGC TCACGCAGGG 780 AACCCCTCAG GCCCGGGTGT GGGAAGCAGG GTGAAGGAGC CCCGACTCTT CGGAGGTCAT 840 GCCCCCAGAG CGCAGGGGAA GGCCGAGTCG GCCACTGCCT GGCTGTTTGC TGGGACGAGG 900 GGATCGAGGG CCTGGCAGGG ATAGTACCTC TGAGACGCCT GCCTCCGGTG CTCCCTCCCG 960 CCGTGCCTCC CTCCCTCGCT CGGTCCTCCG TAGCTCCTAC TGGCGGAAAT CTCAGCAGGC 1020 CCTTTGTTTT CTGTTCCCCA CAGCCTGGGC CGGCTCCTGC CCTCACATAT GCTCCGGCAC 1080 AAGCTGCAGG ACTGCCCCCT CCCCCTCGGC AGTGTACACA TTTACTCTCC TACAGACACA 1140 GCCCCATTGT CTCCGCCACT GCTCTTCCCC GGCCCTCTGG GTTCCAGATG AGGCCAGCTG 1200 AGCCCCCCGA CCCCCCCACA GCTGACCCAC CCTGACTGCC TCGGGAAAGG AGCGGGGGAG 1260 GGGGCCGTCA GGCCGGATTC CTTCCACCAC CTTCTTGGCC CCCCTCTCTG CCACTCCCCC 1320 TCCCGGAAAT CCCCTCTTCC TCTCCCACTC CCACACCCCC TCCCCCCATC CTGTCTTCTT 1380 CCCTGGGCCT TGGCCTCCAC TGCACAGCCT GGAGCAGCCT CTGCCCTGCC TGTCCCCCAT 1440 CCCCCAGTGC CTGAGCTGTG CTGCTGAGGC TTCTGAAGGG GAGAGAGGTG GTTGGGTGGT 1500 CCCTGCTCCT CACCCGCCAC GGTACAAGCA CAAGTGAGGG TGTCCACAGC CCTGGCTGGG 1560 CCCCAAGCTG CAGGCTAAGC TTCTGCCTGA AGCCTAGGGA CTTGCCTCTG TCCCCTCCCT 1620 TTCTCCAAAA CCACTCAGTC AGCACATTCC TGAAGCAGCC AAGTGGACCC CCTCCCCCTG 1680 GGCCCACCCC TCTTTCCCCA CTCCTGCCTG AGCTGTTAGG TTGGCCCAGG AAGGCTGGTT 1740 GCCCTGTGGG CAGACACACC CCTTCAGTGC CTGTGGTTGT ATTGTCCTTG GCATTGAAGC 1800 ATGGCCAGTG GTAGTGGGAT CAAGGGGAGG AGGTGGGTGC TAGAAATCCT TGGGGCAGTT 1860 GGGGCATGGA CTGCCTGGGT CCTGGAGAGT GCCTCTAGAA CTGGGCTCCC ATGTGGGCTC 1920 TGGTTCCGCC TGGATCCCTG CCTGCCTTCC ACCTACCTGA CTCAGACCTG CCAGGAATGC 1980 CCTGCCCCAG GGCCCTGAGT CCTGCTGGGT GAGCCATTGC TCTGCCTGAG CCATGCCAGG 2040 CATGTGTGAC TGGCCCTGGC TGGGGTCAGC AAGGGCATGT CGACAGAAAG AAGCATGCCA 2100 ACAGGCTCCT TGGGTGCTGA CGGCCAGGTA GGGTTTGGTG CAGGAGAAGG CGGGCAGCTA 2160 GCAGGAGGGG ACGGTCACCA GGCTTCAGAA GCCCACTGAG CAGTGCCCAG AGTCTTAGCT 2220 GTGCTTGCTG GACATTTTTC CTTGCCCCAG CTTCTCTTCC TTGTGTGTGT GGTGTAGTAG 2280 AGCCTGTCTG AGCTGTGGAG TCAGACACAC ATAGCCAGGT GCTGCTTCAC CTGTAAGCCT 2340 CTTCGTTTCA TCTGTAAAAT GGGGGCATTC CACCCCTTCT CAGAGGCAGG TGGCAAGGGC 2400 CGGGTGGGAA TGTAAACAGG TGCCAAGGAG CATGCCTTTC CTCCCCTTTT CTGTGGGAGA 2460 CACACCCTCA AAGGAGCAGG GCAGGGTAAG GTGGCCGCAA GCTGACCTTT GCCCTGGTTC 2520 TTGGCAGAGG ACCTTCCTGG GGACTGGGCA GCCTTCGCAC TTAATCTCAG CCCATCCCTG 2580 TTCCCCCTCC CAGTCAGCTT TCAGCGCAGC CAATGAAAAC TAACCTAGGG GGAGGGGGTG 2640 ACTGTGCAGC GTGTTCCTTT CCCAGTCCAG CTGCCATCCT GGGGGAGGGG GTGCCAGCTG 2700 CCACCTGTTG GCCAAGTCCT GACTGAGGCA GCTGTCTGTG CCTCCTCTAG GCCCAGACCC 2760 CCCTTCCCAG GACAGGGGCT GGGGTCTTCT GGGATCCTGG GGAAGTAGAG CCCCTCAGGC 2820 CTCTGCTTGC CCTTTTGTCT CATCTAGGCT GGTTGGGAAC CGGTCTGGTG AGGAAGGGAG 2880 GCTGCCTCAG TGGAGGGGGT GGGGCCAGGC CTCCCTTTCC CCTAATGAGA AACCTTTTTC 2940 CTGCCCCTCC CCCATTTCAG 2960
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