Tag | Content |
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EnhancerAtlas ID | HS093-26297 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr6:26171700-26173920 |
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 | ATGTGGCTTT GGTAATGAAC CTGAAGTTAA AAACTGGTTA GCTTATGCTA AGCTGCCATT 60 TGAAAGGTCT CCTCCAGCAT CTGAATTAAG GGAAACAATG TTTTGAAGCA GTCACAAAAC 120 TTTTCTGATG CATTAGATCT GAGGTAGGAC CTGATAATTT GTACTTCTAA ATTATGCAGG 180 TGATGCTGAT GCTGCTGGTC CGGAGACCAC TTTGGAGAGT TTTACTTTAA AGGAAATGAA 240 ACTGCCCTAA AATGCTAATA CTAAATAGCC ACACAAAGCC GGAAAAAAGC AAAGAATTTC 300 AAACCGAAGA TGAGAGGTCC TGAAAAATAA CAGCGGTCAT CCTACTCCCG GTGCGGCTAT 360 GCGGCCATGA AAAGGAGTCT TGGGGCCGGT CGTGCCCCTC CACGCAGGCT CCCTCATAGG 420 GTCATCCCAT CAACCCTCGC CAAAAACGCC GGCCCCCTCA TAGGGCCGTC CGGCCACGCC 480 CCTCCGTGCC CTAACCACAG AGCCACACGT TACGCCGCCG CCCCGTTACG CCCATCCGGC 540 TCCCGCATAG GGCGTCACGT ACGTTTAACG TCGGCCCGGC GCGCGCGTCC GGGAGGTTGC 600 CCGTAGGCCG CTAACTGGTG GTTCCCAGTC CCCGCCGACT CGGCCTCTTT CTTCTGCGGC 660 CACCAGATCG CGGGATATCG GAGACTTCGA ACAATCCGCT GGAGTCCTTT ACAGTTTAAA 720 AACAGAGGAC CGGCCGGGCG CGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCCG 780 AGGCGGGCGG ATCACGAGTT CAGGAGATAG AGACCATCCT GGCTAACACC GTGAGACCCC 840 GTCCCTATCA AAAGTACAAA AAAATTAGCC GGGTGTGGTG GCACGCGCCT GTAGTCCCAG 900 CTACTCAGGA GGCTGAGGCA GAAGAATCGC TAGAACCAGG GAGGCGGAGG TTGCAGTGAC 960 CGAGATCGCG CCGCTGCACT CCAGCCTAGG CGACAGAGCG AGACTGCGTC TCAAAACAAA 1020 AAAAACGGAG GATCGAAAAT TTTGAAGACT GAGAGCAAGG CAACAATCTT CCCTTGACCT 1080 TTTTGCTCCT CTCACAAGGG TTTTTCAGAC GGCTGAAACC AACGAAAAGA GTGAGGAAGC 1140 AGGCAGAAAA TTTCAGCTTT AGTCTCTCAG CATCCTCCTG CTTTCTTCTC GGGGAGCTGG 1200 CACTTCCCCC TTCTCTAGTA GCTGTAAATA CGCCTCCCAA CTCCAAGGAG ACCTTTCTTG 1260 CATCTCCCTT ACTGTTCTCA CGCCTGTAGG GCTCTTCGTG TGAGGATTCA GTGTATGTAT 1320 GTATGTATAT GAATGTGTGC GAATAATTAT TTCCTAATTG AGTTTTTTTT TAAAAAAATC 1380 ATCTTCCGGT ACACGCAGTG CCGTACTCCA TTAAACAGCA GGCACGGTGT CTAGGGTCCG 1440 CAGTTCTTTT GGAGGCTCAT GAAAATATTT TAATTTCTTC TAAAGTCAGA AGGAAAAAAA 1500 TGAACATTTA AGTCGAAGAA GATGTTACAT ATTAATCTTC ATATGACTTT AATTTTTTTT 1560 TTTTTTTTTT TGAAACGGAG TCTCGCTCTG TCCCCCAGGC TGGAGTACAG TGGCGCAGTC 1620 TCGGCTCACT GCAAGCTCTG CCTCCCGGGT TCACGCCATT CTCCTGCCTC AGCTTCCCGA 1680 GTAGCTGGGA CTACAGTCAC CACGCCCGAC TAAGTTTTTT TGTATTTTTT AGTAGAGACG 1740 GGGTTTCACC GTGTTAGCCA GGATGGTCTC GATCTCCTGA CCTCGTGATC CGCCCGCCTC 1800 GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACAAC GCCTGGCCTA TGCCCACTAA 1860 TTCCAATTCT TATTTGATCT AATTGTTTAT AGATTCTTGT GAACTTTTAC CTTGACAATT 1920 ATGTTATTTT CAAAGATAAT CATCTTTTCC TATTGAATCC TTGCTCTTCT GACTGCCTGT 1980 TCCTATCTCA TGGTATTGGC CAAACCCTGT GATGCCGTGT TGAATAGGAG TACTTTCTCA 2040 CCACACTTGT CTTCCTTCCG CCTCTATGGG AATCCTTCCA AAACGGCACC ATTAAGTGTT 2100 ATACTCGCTG TAGCTCCTCC TTATGAAGTT CTCTTCTCAT TGTAGTCTGT TAAGTGTTTA 2160 TGATTAAAGA GTGTTATATT TTGTTAAATG CTTTCGCAGT ATCTTTGGAG ATGATCATGT 2220
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