Tag | Content |
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EnhancerAtlas ID | HS109-19392 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr6:26173400-26173870 |
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) |
Nkx3-2 | MA0122.3 | chr6:26173848-26173861 | GTTAAGTGTTTAT | - | 6.08 | Zfx | MA0146.2 | chr6:26173492-26173506 | CCCGCCTCGGCCTC | + | 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 | CACGCCCGAC TAAGTTTTTT TGTATTTTTT AGTAGAGACG GGGTTTCACC GTGTTAGCCA 60 GGATGGTCTC GATCTCCTGA CCTCGTGATC CGCCCGCCTC GGCCTCCCAA AGTGCTGGGA 120 TTACAGGCGT GAGCCACAAC GCCTGGCCTA TGCCCACTAA TTCCAATTCT TATTTGATCT 180 AATTGTTTAT AGATTCTTGT GAACTTTTAC CTTGACAATT ATGTTATTTT CAAAGATAAT 240 CATCTTTTCC TATTGAATCC TTGCTCTTCT GACTGCCTGT TCCTATCTCA TGGTATTGGC 300 CAAACCCTGT GATGCCGTGT TGAATAGGAG TACTTTCTCA CCACACTTGT CTTCCTTCCG 360 CCTCTATGGG AATCCTTCCA AAACGGCACC ATTAAGTGTT ATACTCGCTG TAGCTCCTCC 420 TTATGAAGTT CTCTTCTCAT TGTAGTCTGT TAAGTGTTTA TGATTAAAGA 470
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