Tag | Content |
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EnhancerAtlas ID | HS164-08440 |
Organism | Homo sapiens |
Tissue/cell | Raji |
Coordinate | chr22:47129850-47132900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EN2 | MA0642.1 | chr22:47132290-47132300 | GCTAATTGGG | - | 6.02 | FOXC1 | MA0032.2 | chr22:47130644-47130655 | ATATTTACATA | - | 6.62 | Foxa2 | MA0047.2 | chr22:47130464-47130476 | TGTTTACACAGG | + | 6.14 | RREB1 | MA0073.1 | chr22:47130966-47130986 | CCCCCCAACACACACACACA | + | 6.69 | RREB1 | MA0073.1 | chr22:47130968-47130988 | CCCCAACACACACACACACA | + | 7.29 | SOX10 | MA0442.2 | chr22:47131413-47131424 | AAAACAAAGGA | + | 6.32 | Sox3 | MA0514.1 | chr22:47131413-47131423 | AAAACAAAGG | - | 6.02 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_09349 | chr22:47130192-47135971 | CD14 | SE_14697 | chr22:47130289-47135628 | CD4_Memory_Primary_7pool | SE_17674 | chr22:47129977-47136955 | CD4p_CD25-_CD45RAp_Naive | SE_17901 | chr22:47129479-47137350 | CD4p_CD25-_CD45ROp_Memory | SE_18695 | chr22:47129530-47134167 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19505 | chr22:47129264-47136199 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20325 | chr22:47129975-47135578 | CD56 | SE_23520 | chr22:47130719-47132305 | Colon_Crypt_1 | SE_24287 | chr22:47130679-47131949 | Colon_Crypt_2 | SE_27442 | chr22:47130654-47136087 | Esophagus | SE_28432 | chr22:47129751-47141198 | Fetal_Intestine | SE_29215 | chr22:47129758-47141281 | Fetal_Intestine_Large | SE_31641 | chr22:47129922-47130667 | Gastric | SE_31641 | chr22:47130718-47135958 | Gastric | SE_38281 | chr22:47129860-47135670 | HUVEC | SE_40789 | chr22:47129770-47139213 | Left_Ventricle | SE_42260 | chr22:47130597-47139109 | Lung | SE_48916 | chr22:47130614-47133016 | Right_Atrium | SE_49561 | chr22:47130813-47132963 | Right_Ventricle | SE_50233 | chr22:47130014-47135867 | Sigmoid_Colon | SE_51682 | chr22:47130699-47137805 | Skeletal_Muscle | SE_52427 | chr22:47129806-47136051 | Small_Intestine | SE_53517 | chr22:47130708-47132392 | Spleen | SE_53517 | chr22:47132592-47135794 | Spleen | SE_58383 | chr22:47122081-47199614 | Ly1 | SE_62483 | chr22:47129710-47188820 | Tonsil | SE_65427 | chr22:47130748-47133722 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr22 | 47130002 | 47130258 | chr22 | 47130333 | 47131449 | chr22 | 47130063 | 47131516 |
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Enhancer Sequence | TGAACCCGGG AGGTGGAGGT TGCAGTGAGC CGAGACCTTG CCACTTCACT CCAGCCTGGG 60 AAACAGAGGA AGACTCCAAA AATATAATAA AATATGTTAT ATATACATAC ATACATATAT 120 ATATATATAT ATATACATTT TCCTATAATC CAGCTTTCTA CTCTTAAATA TGCACCCAAG 180 AGGAGCAAAA GCATAGCCCC TAAAGGGTCA GGGTGTCTTT ATCCACATAG TCAAGGTGAA 240 TGGACTGCAA ACTGTCCAGA AGCCCATCAG CAGGTGAACG GATACACTAG TGCACCCACA 300 CAATGCAATA TGACTTAGTA ACCAGAAAGA AGGAACTGCT GACATGATGA ATCTTAAAAA 360 AAACAAAATG AGATAAAGCA GCCGGGCACA AAGACGTGCA CATGGCATGA TTCCATTTAC 420 ATGAGATAAA GCAGCCGGGC ACAAAGACGT GCACATGGCA TGATTCCATT TACATGAGAT 480 AAAGCAGCCG GGCACAAAGA CGTGCACATG GCATGATTCC ATTTACATGA AACTCTATTA 540 GCATCGTGCC TGTCCCTGGT GAGAAAACAG CCCAGGGCCC AGGAGAAGGT GCTGGGCTGC 600 TGCGATCCGG GTGATGTTTA CACAGGTGCA CACAATTATC AAAATTTAAC CAACTATGTG 660 CCTTAAAATG TCTGAGTTTT ATTGCATGCA ATTTAGACCT TGATAAAATC GATTTTTAAA 720 AATCATGTCT TAGGAGAGGA ATTAGTAGCG TGGAAAACAC TCTGCAGTAT GTTTTCTCAG 780 CTTTTCTTTC ATGCATATTT ACATATACAC AAATACCAAA TATTAATCAC GTCTAAGTCG 840 AAGAGTGACT TTTTGTGTAT GCTTTTCTGT GTTTTCTCGA TATTATTAAA TCAACATGAC 900 TTACTTTTGT AAGCAGGAAA AACATTTTTT TAAAGTATCT GTGGCATGCC TATGTTTTGC 960 CAGGCACTTT GCAGGGTGTG CTGAGGACAC GCTTTATAAA CACAGTACTG ACCTGCCCAA 1020 CGAGTTCACC ACCAGCCTGG GACATCCCAA GTGGGGTTGG TGGAAGGAAG GGGAGGATCC 1080 TCCCACAAAG GTAGAGCCTG GGCAGTAGTC CCCTCACCCC CCAACACACA CACACACACA 1140 CACACACTCT TCCCATTCCC AACTCTAAAG GAATAAATGC AGGGTTTGTC TAAGTGTGTT 1200 TTGCGACAGT CAGGGGAAAT AACCCAGATA TCAACTCAGT GTTTCCAGTT CAACGAGCAT 1260 GACCCACTTC AAGTTCCTGT TTTCGTCCTG CCCTACTTCC CACCAGGCTG GCGGCCCAGG 1320 GCACTTGCTG TCGCGGCTTC CTCAGGTGCA GACCTCACCC AGGCCCAGGA AGCTGCAGCG 1380 ATCCAAATTG CTAGTCCTTG TCTGTGCTCT TGTACAGTCA GTCACTGTCC CAGCATGATG 1440 ACCCACTGAC GAAAGTGCAC GTGCCTGGGT TCAAAGCCAG CTCCCTCTGT ACATCACTGC 1500 CTCTGGGCCC AGTCAATTCC CACTCCTACT GTCCACATCT GAAATAGGGG TGATGCTACG 1560 GAGAAAACAA AGGAGTCGGA ATAACTAAGC GGCCACCCCA GCAGGGCACA CACAGTGGCC 1620 TTGGCTTTGT CTTTAGCCCA TTGGTCACCT GGAGCTCCAG GGCTGCTCCT GCCTCATCTC 1680 ACAGGTCCTC CTAGGGCCAG TTTTTGCACA ATTCTCCACC TCTCATCATT CCTCAACCTA 1740 ATCAATCCCA GTGTGCCCAG ATACACCTGG GGGAATGGGG AGGGCTGGGC AATGCCACCT 1800 TGCTGACCAA ATTAAATGTC CTGTGAGCTG GTTCACATTC TTCTGCCCTA CTATGGCCCT 1860 ACTGACCTCA AGCATAGAAG AATCGAACCT GGGCCTGATT CCTTTTGGGG ACTGTAAAGC 1920 TATGAGAAAA AAACTAGAGA CAGTGTGGCT GTATTCCTGA ACTCATTCAC AACTTAGCGT 1980 TTCCCAACTT GTTGATGTTT TCCCATTGCA TGGGAGAGCA CTCCTGGGTG GAGAGGGCAG 2040 GCTGCTTCCT GGAGGAAGCC CACCAGCCAG GGCCACCAGC CAGGGCCCCA CCATCCATGG 2100 CCCCACAAAC CAGGGCCCTC CCTCTCCAAG AGGGACCAAG CTCCTGGCAG GCCAGTCAGG 2160 CAGCTCAGGA TGAACCCGCA CAAAAGCACC TTGGCTTAGC AAGAGTGAAG CAATTAGCAT 2220 GCCAAGAGGC AAACCCCAGC AGGCTGGACA AAAGCAGACG CCACACCACA CCAAGCCCTG 2280 ACCTGGGGGA CCAGAAACCA TAATGGGAGC TGGCTGGGGA CGCCAAGGCA GAAAGCAGTG 2340 ATGACTGACC TCCCACACAG ATGCCCTGTA AGGGTCTGGC GTCTCTGCGG CGGCTGGAGC 2400 CTGAGGGAAG CCTTACAGCC CAGTGGCTAC AAGCACAGCA GCTAATTGGG CCAGTCACTT 2460 CCAGCCCCTG CAGATCGGCC CCTGCATCCC TAGGACGGGA GCAGCTGCCT CTCAGGAACC 2520 CATCCGGTTT GAAGCCCAGT GGCCCGCACT TAGGAAGTGC TTGGGGGAGG CAGTCATCTT 2580 CCTGAAGCCT AGGGATTTAC AACAAAGTAC AAACCCTTCG GGCCCAGGTC AGGCACCTGT 2640 TCTCCTTGTG TGTGGGCCCT GGTGGGTGAT ATTTGGGGTG TGACATTTCT ACCAAAGGGG 2700 ACATGAGAAA TACCTTAGGA AAGTCAAGTC TCAGATGCCC AGCCACAGAT AGGTGACCCC 2760 AGGGCTGGAA ACCAAGTGTT GGTCATGGGT CTGAGACCAC CCCTCGACCT TGGCCCCACC 2820 TAACGTTCAA CTCTGTCCCC ACCAGAACCC AACCCACAGA TCCTCACCAC TCAGCACCAG 2880 AAAGCGCCCA GAAGAACTCC TGACCTCGAC TGCCCACAGG GTCTAAAGGT GTCATCCCAG 2940 GCTCCGAATA TCCACCAGAG AATCTTGGCC TCCGCCACAC CCACCCCATT CCAGCTCCGC 3000 ACATCCAGCA TGAATCCTGG CCTCTGCCAC ACCCACCCCA ATAATTAAAA 3050
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