Tag | Content |
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EnhancerAtlas ID | HS183-07293 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr6:26171570-26174020 |
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) |
KLF14 | MA0740.1 | chr6:26172171-26172185 | GGCCACGCCCCTCC | + | 6.25 | NR2F1 | MA0017.2 | chr6:26172770-26172783 | CCCTTGACCTTTT | - | 6.39 | Nkx3-2 | MA0122.3 | chr6:26173848-26173861 | GTTAAGTGTTTAT | - | 6.08 | SP3 | MA0746.2 | chr6:26172171-26172184 | GGCCACGCCCCTC | + | 6.18 | Zfx | MA0146.2 | chr6:26173492-26173506 | CCCGCCTCGGCCTC | + | 6.01 | Zfx | MA0146.2 | chr6:26172473-26172487 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_12258 | chr6:26170126-26174148 | CD3 | SE_15406 | chr6:26170232-26174130 | CD4_Memory_Primary_8pool | SE_15814 | chr6:26170484-26173824 | CD4_Naive_Primary_7pool | SE_16410 | chr6:26169818-26173905 | CD4_Naive_Primary_8pool | SE_17748 | chr6:26169679-26175030 | CD4p_CD25-_CD45RAp_Naive | SE_20332 | chr6:26169424-26174488 | CD56 | SE_21497 | chr6:26170679-26173958 | CD8_Naive_7pool | SE_21986 | chr6:26169898-26174317 | CD8_Naive_8pool | SE_22908 | chr6:26169277-26174695 | CD8_primiary | SE_26174 | chr6:26170640-26174359 | Duodenum_Smooth_Muscle | SE_27280 | chr6:26171109-26173883 | Esophagus | SE_28057 | chr6:26171011-26174124 | Fetal_Intestine | SE_29032 | chr6:26170881-26174023 | Fetal_Intestine_Large | SE_29729 | chr6:26170976-26174103 | Fetal_Muscle | SE_32034 | chr6:26171514-26173635 | Gastric | SE_40402 | chr6:26171125-26174414 | K562 | SE_42987 | chr6:26171339-26173866 | Lung | SE_50620 | chr6:26171127-26173936 | Sigmoid_Colon | SE_52776 | chr6:26171093-26173968 | Small_Intestine | SE_53423 | chr6:26171175-26174177 | Spleen | SE_61788 | chr6:26155157-26176422 | Toledo | SE_62340 | chr6:26155053-26176655 | Tonsil | SE_65079 | chr6:26171576-26174025 | NHEK | SE_66906 | chr6:26171236-26174194 | H2171 | SE_67155 | chr6:26169999-26173929 | MM1S | SE_67973 | chr6:26087132-26287126 | TC32 | SE_68399 | chr6:26087114-26175354 | TC71 | SE_68400 | chr6:26087114-26175354 | TC71 | SE_68401 | chr6:26087114-26175354 | TC71 |
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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 | TTGTAAATTC TGCCTTCATT GTTGATCCAA ACCTTTCTTC TAAGACCTCC CCTTTCTAGA 60 CATCTATCTA CCTATTTTCA CTTTACTTTC CAGCATCAAG GAGGTCTGAG TGGATAAGGC 120 CTAAGCACTG ATGTGGCTTT GGTAATGAAC CTGAAGTTAA AAACTGGTTA GCTTATGCTA 180 AGCTGCCATT TGAAAGGTCT CCTCCAGCAT CTGAATTAAG GGAAACAATG TTTTGAAGCA 240 GTCACAAAAC TTTTCTGATG CATTAGATCT GAGGTAGGAC CTGATAATTT GTACTTCTAA 300 ATTATGCAGG TGATGCTGAT GCTGCTGGTC CGGAGACCAC TTTGGAGAGT TTTACTTTAA 360 AGGAAATGAA ACTGCCCTAA AATGCTAATA CTAAATAGCC ACACAAAGCC GGAAAAAAGC 420 AAAGAATTTC AAACCGAAGA TGAGAGGTCC TGAAAAATAA CAGCGGTCAT CCTACTCCCG 480 GTGCGGCTAT GCGGCCATGA AAAGGAGTCT TGGGGCCGGT CGTGCCCCTC CACGCAGGCT 540 CCCTCATAGG GTCATCCCAT CAACCCTCGC CAAAAACGCC GGCCCCCTCA TAGGGCCGTC 600 CGGCCACGCC CCTCCGTGCC CTAACCACAG AGCCACACGT TACGCCGCCG CCCCGTTACG 660 CCCATCCGGC TCCCGCATAG GGCGTCACGT ACGTTTAACG TCGGCCCGGC GCGCGCGTCC 720 GGGAGGTTGC CCGTAGGCCG CTAACTGGTG GTTCCCAGTC CCCGCCGACT CGGCCTCTTT 780 CTTCTGCGGC CACCAGATCG CGGGATATCG GAGACTTCGA ACAATCCGCT GGAGTCCTTT 840 ACAGTTTAAA AACAGAGGAC CGGCCGGGCG CGGTGGCTCA CGCCTGTAAT CCCAGCACTT 900 TGGGAGGCCG AGGCGGGCGG ATCACGAGTT CAGGAGATAG AGACCATCCT GGCTAACACC 960 GTGAGACCCC GTCCCTATCA AAAGTACAAA AAAATTAGCC GGGTGTGGTG GCACGCGCCT 1020 GTAGTCCCAG CTACTCAGGA GGCTGAGGCA GAAGAATCGC TAGAACCAGG GAGGCGGAGG 1080 TTGCAGTGAC CGAGATCGCG CCGCTGCACT CCAGCCTAGG CGACAGAGCG AGACTGCGTC 1140 TCAAAACAAA AAAAACGGAG GATCGAAAAT TTTGAAGACT GAGAGCAAGG CAACAATCTT 1200 CCCTTGACCT TTTTGCTCCT CTCACAAGGG TTTTTCAGAC GGCTGAAACC AACGAAAAGA 1260 GTGAGGAAGC AGGCAGAAAA TTTCAGCTTT AGTCTCTCAG CATCCTCCTG CTTTCTTCTC 1320 GGGGAGCTGG CACTTCCCCC TTCTCTAGTA GCTGTAAATA CGCCTCCCAA CTCCAAGGAG 1380 ACCTTTCTTG CATCTCCCTT ACTGTTCTCA CGCCTGTAGG GCTCTTCGTG TGAGGATTCA 1440 GTGTATGTAT GTATGTATAT GAATGTGTGC GAATAATTAT TTCCTAATTG AGTTTTTTTT 1500 TAAAAAAATC ATCTTCCGGT ACACGCAGTG CCGTACTCCA TTAAACAGCA GGCACGGTGT 1560 CTAGGGTCCG CAGTTCTTTT GGAGGCTCAT GAAAATATTT TAATTTCTTC TAAAGTCAGA 1620 AGGAAAAAAA TGAACATTTA AGTCGAAGAA GATGTTACAT ATTAATCTTC ATATGACTTT 1680 AATTTTTTTT TTTTTTTTTT TGAAACGGAG TCTCGCTCTG TCCCCCAGGC TGGAGTACAG 1740 TGGCGCAGTC TCGGCTCACT GCAAGCTCTG CCTCCCGGGT TCACGCCATT CTCCTGCCTC 1800 AGCTTCCCGA GTAGCTGGGA CTACAGTCAC CACGCCCGAC TAAGTTTTTT TGTATTTTTT 1860 AGTAGAGACG GGGTTTCACC GTGTTAGCCA GGATGGTCTC GATCTCCTGA CCTCGTGATC 1920 CGCCCGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACAAC GCCTGGCCTA 1980 TGCCCACTAA TTCCAATTCT TATTTGATCT AATTGTTTAT AGATTCTTGT GAACTTTTAC 2040 CTTGACAATT ATGTTATTTT CAAAGATAAT CATCTTTTCC TATTGAATCC TTGCTCTTCT 2100 GACTGCCTGT TCCTATCTCA TGGTATTGGC CAAACCCTGT GATGCCGTGT TGAATAGGAG 2160 TACTTTCTCA CCACACTTGT CTTCCTTCCG CCTCTATGGG AATCCTTCCA AAACGGCACC 2220 ATTAAGTGTT ATACTCGCTG TAGCTCCTCC TTATGAAGTT CTCTTCTCAT TGTAGTCTGT 2280 TAAGTGTTTA TGATTAAAGA GTGTTATATT TTGTTAAATG CTTTCGCAGT ATCTTTGGAG 2340 ATGATCATGT TTTTTCTTTA TTAATCTCTT TTTTATTTTA TTTATTTTAT TTTATTTTAT 2400 TTTATTTTTT ATTATTTTAG TTTTTATTTT GAGATGGAAT CTCACTCTGT 2450
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