Tag | Content |
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EnhancerAtlas ID | HS093-16721 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr2:43436560-43439120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr2:43436583-43436594 | GGGCGGGAAGC | + | 6.02 | Myog | MA0500.1 | chr2:43439024-43439035 | CTGCAGCTGTT | - | 6.02 | Tcf12 | MA0521.1 | chr2:43439024-43439035 | CTGCAGCTGTT | - | 6.62 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_00296 | chr2:43437036-43438790 | Adipose_Nuclei | SE_02969 | chr2:43437301-43438552 | Bladder | SE_09435 | chr2:43435994-43442184 | CD14 | SE_13297 | chr2:43437195-43438199 | CD34_Primary_RO01480 | SE_13409 | chr2:43436855-43438842 | CD34_Primary_RO01536 | SE_14384 | chr2:43437082-43438015 | CD4_Memory_Primary_7pool | SE_23059 | chr2:43435636-43436863 | Colon_Crypt_1 | SE_23059 | chr2:43437029-43438580 | Colon_Crypt_1 | SE_23724 | chr2:43437108-43438529 | Colon_Crypt_2 | SE_24685 | chr2:43437071-43438522 | Colon_Crypt_3 | SE_25333 | chr2:43435716-43436820 | DND41 | SE_25333 | chr2:43437248-43438244 | DND41 | SE_26557 | chr2:43435567-43436848 | Esophagus | SE_26557 | chr2:43436992-43438585 | Esophagus | SE_27617 | chr2:43437101-43438574 | Fetal_Intestine | SE_28536 | chr2:43437132-43438609 | Fetal_Intestine_Large | SE_30898 | chr2:43437035-43438523 | Fetal_Thymus | SE_31392 | chr2:43437058-43438494 | Gastric | SE_42201 | chr2:43437107-43438599 | Lung | SE_49954 | chr2:43435662-43436925 | RPMI-8402 | SE_49954 | chr2:43437061-43437837 | RPMI-8402 | SE_49954 | chr2:43437929-43439181 | RPMI-8402 | SE_50052 | chr2:43437129-43438588 | Sigmoid_Colon | SE_52337 | chr2:43437228-43438505 | Small_Intestine | SE_53288 | chr2:43437488-43438534 | Spleen | SE_54937 | chr2:43437479-43438753 | Stomach_Smooth_Muscle | SE_55103 | chr2:43437454-43438410 | Thymus | SE_61450 | chr2:43354337-43468354 | Toledo | SE_62203 | chr2:43354169-43468733 | Tonsil | SE_65350 | chr2:43437314-43438678 | Pancreatic_islets | SE_68698 | chr2:43437173-43438588 | 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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| Number: 2 | ID | Chromosome | Start | End |
GH02I043208 | chr2 | 43435568 | 43436925 | GH02I043209 | chr2 | 43437114 | 43439109 |
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Enhancer Sequence | GGCACTATGT TGGGGAAGGT GGGGGGCGGG AAGCAGGAGA GTTGCTGCTC CCCAAGAGCC 60 TGGAGGTGTG GGGAAATGGG GCTCAGCCAC GGGAGATTGT GAATACAGGT TCTGCCACCA 120 GCCACTTCTA GGCGTGGCTG CATAACCGTG GATGATTCAC TTAACCTCTG TCTGCTGGGG 180 TTCTGGCTCC CATGATGGTT AGAACACCAC CTTCTAGGAT TGGTTCAAGG ATGGCATGGC 240 ATAATAAGAA CACTTTGAGG GAGGGGGTTT GACAGAGTAT ACTCCATAAA TTATGGCCAC 300 TGTTATTATT ATTATTATTG AGATGGAGTC TCAGTCTATC ACCCAGGCTG GAGTGCAGTG 360 GCGCAATCTC AGCTCACTGC AACCTCCGGC TCCCAGGTTC AAGTGATTCT CCTGCTTCGG 420 CCTCCCTAGT AGCTGGGATT ACAGGCGCGT GCCACCACGC CCAGCTAGTT TTTGTATTTT 480 TAGTAGAGAC AGGGTTTTGC CATGTTGGCC AGGCTGGTCT TGAACTCCTG ACTCAGGTGA 540 TCCTCCCGCC TCAGCCTCCC AAAGTGCTGA GATTACAGGT GTGAGCCACT GCACCTGGCC 600 ATGGCCATTA TTCTTAAAAC GAGCAACTGG AGAACAGGGG ACTATTGAGC TTGGCCAGAT 660 GTCCAGCTAT GTATCCACAG GGGCCTCAGG AGTTTTCAGA GTGGGGAGCA AGGCCTCTGG 720 CCTGGAGCAG ACAGGGCTGC TTCCTAGAAG AGGAAGCCTC AGGTGCCAGG CTGAAGGGCT 780 GGAAACTGGG AGCTGGTGGG AAGGAAGGTG TCTGGGCCAG GATGTGGAGT GGGGCAGGGA 840 GGAGGTGCGC CTTTGAGTGT ATGTGAGAGA GACAGAGACA GCTGGCCCTG AGGCCACCGT 900 ACAGGTGTGA ACAGGTGAGC CGTGAACCCC ATGCTGATTC TTTGCAGGGC AAGGGGCTCC 960 TATGCCAGGG AGAGGCCTCT GGGACACAGG AGCGCTGTGG GGTAGGGAAG CCTGCACGCC 1020 TCACACGTGG GGGATGCATG GCCTGCAACT GACCAGAAGA AGCCCAGTTA GGCCCTGGCT 1080 GGGCTCTCCT TTGGTGCTAT CCCTTGGGCC AGTATCAAGA GCTGCAGATG TGCACGCCTA 1140 TGGAGCTCTT GGGAGCCTCA GCCCTCACGC CCCCATCATC ACCCCCCAGC CAGCCCACGG 1200 GGCCTCAGGT GGCGGGAAGG CAGGACCGCA GGGCCTGTGG CAGGGCAGGG AAAGGCACGG 1260 AATGGTGTTT ACATTTTCCC TCCTTCCCTG CTGGCCTGGC GGTTACACCA CTGCGGTTTG 1320 TTGGCCCCAG GGAGCGCCTC CCTTACATAA CGCCTGACAT AACTGCCCTA AAACACACGC 1380 ATGGCAACTC CCACATAGCA CCACACATGC TGTCATGCCG GCTCACCCCC CCACACTCAC 1440 ACACACTCAC AGAGCCACAC CACAGCCTCA CGCACTCACA CACACACACC CCTTCCCACA 1500 CACGCTGTCA TCCCAATGCT GTCATTTCAG AAAGGATTTC TTTTGCTCCC ACCACCCATC 1560 ACACAGGCAG GGCCTCCCCG ACGTGGCTTC AGTGCCTCTG GTTCCTCAGG CCCCAGGAGC 1620 CCTGAGCCCA CTGGGACTGC TCCAGGCCTC GCCTGGGTCT CCCAGGTGGC AGCCTCAGAC 1680 TGTGGTGCCA GCCTAGGCAG TGGACGACAA CAGGGGGACT TGAGAACAGG GCAGGGAGTC 1740 GGAGAAAGAC CAGAGTCCAG GCTGGAGCCC CTGAGATGTG GACTCCAGAA ACTCAGAACA 1800 GGCAGTGGGG AGGGACAGAC AGGGAGGGAC GCGGCCTCCG AGGTATTATA CTTAGTGCAA 1860 CATGTTACTA CGAGGGCAGG CTTCAAGCAT TTAATGCATG ATGGGCCAGG CGCAGTGGCT 1920 AACGCCTATA ATCCCAGCAC TTTGGCAGGC CGGAGGATGG CTTGAGCTCA GGAGTTCGAC 1980 ACCAGCCTGG ACAACATAGC GAGACCCCCT GTCTATAAAA AATAAAATAA TACTATAAAT 2040 TAGGAAAAAT GCATGTGACC CTCCCAAGAA ACACGTGAGC CACACTGTGA CCCATGCATG 2100 CTACTTCTCG GGATTCATCT GATGGAGATA TTCACCCAAG GCCCTGAGTT AAAAAAACGT 2160 TCATGCTGCA ATGTTGGTAA AAGCAAAATA ATGCAGAGCC TCCCTGTCCA TCCCCTGGAC 2220 CCTCACAAAC AGAGCCACAT GCAGCCATGT TCCAATGCCC TAAATGATAG GTCAGGGGAG 2280 AGAATGACCC CATTTTGTGA CTGAAACCAT ATATGAATGT GTGTGTATAA ATATTTGTAG 2340 ATAGGTGCCT CACCAGATCT CTGGAATGCC TTACACAAAG TGGCCACAAA GTGGCCACAT 2400 TTGCTGAGTG GGCCTGAGGA GGAAGGTTAA GGGGGCCTTT TCCACTTGCA CGTATTGGGA 2460 TTCACTGCAG CTGTTGGAAT ATTCATAACA AGCAGGCATG AGTTCCAAAT AAGAGGAAAA 2520 AATTGGCCAG GAGCGGTGGC TTACACCTGT AATCCCAGCA 2560
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