Tag | Content |
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EnhancerAtlas ID | HS105-14802 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:68120010-68123350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr11:68121263-68121275 | GTGCACGTGGCC | - | 6.22 | Myod1 | MA0499.1 | chr11:68123263-68123276 | AGGAACAGCTGCA | - | 7.34 | Myog | MA0500.1 | chr11:68123266-68123277 | AACAGCTGCAG | + | 6.02 | Tcf12 | MA0521.1 | chr11:68123266-68123277 | AACAGCTGCAG | + | 6.62 | ZNF263 | MA0528.1 | chr11:68120907-68120928 | GGGAGAGGGAGAGGGAGAGGA | + | 6.53 | ZNF263 | MA0528.1 | chr11:68120905-68120926 | GAGGGAGAGGGAGAGGGAGAG | + | 6.5 |
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| Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
SE_01084 | chr11:68120238-68123276 | Adrenal_Gland | SE_01626 | chr11:68117738-68123478 | Aorta | SE_23171 | chr11:68122194-68122741 | Colon_Crypt_1 | SE_23847 | chr11:68121803-68122147 | Colon_Crypt_2 | SE_24963 | chr11:68121832-68122798 | Colon_Crypt_3 | SE_26848 | chr11:68118376-68123358 | Esophagus | SE_28000 | chr11:68120995-68122668 | Fetal_Intestine | SE_28937 | chr11:68120260-68122935 | Fetal_Intestine_Large | SE_30440 | chr11:68120529-68122975 | Fetal_Muscle | SE_31879 | chr11:68119764-68123038 | Gastric | SE_41339 | chr11:68118685-68123382 | Left_Ventricle | SE_41686 | chr11:68120735-68123366 | LNCaP | SE_42205 | chr11:68117678-68123483 | Lung | SE_47270 | chr11:68119431-68123424 | Panc1 | SE_47593 | chr11:68120880-68122853 | Pancreas | SE_48658 | chr11:68117684-68123263 | Right_Atrium | SE_52526 | chr11:68119518-68123360 | Small_Intestine | SE_54745 | chr11:68118516-68123521 | Stomach_Smooth_Muscle | SE_56733 | chr11:68121542-68123099 | VACO_400 | SE_65630 | chr11:68121109-68123518 | Pancreatic_islets | SE_68821 | chr11:68120613-68123171 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 68121765 | 68121884 | chr11 | 68121174 | 68122354 | chr11 | 68120787 | 68122152 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I068352 | chr11 | 68119993 | 68123322 |
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Enhancer Sequence | TCAGTCGGGA GGTGCTAGGT GATTTGTTGG GAGGTGCATG ATGCTCAGTT GGGAGGTGCT 60 AGGTGCTCGG TTGGAAGGTG ATTGGTACTT TGTTAGGAGG TGCTTGGCGC TTGGTTGGGA 120 GTTGTTGGTG TCCAGTTGAG AGGTGCTAGG TGCTTGGTTG GGAGGTATTT GATTGGGAGG 180 TGCTTGGCAC TTGGTTGGGA GGTGCTCTGC ACTTGGTTGG GAGGTGCTCG GTGCTAGGTT 240 GGGAGGTGAT CAGTTGGGAG GTGCTAGATG CTCTGTTGGG AGGTGCATGA TGCTCAGTTG 300 GGAGGTGCTA GGCGCTTGGT TGGGAGGTAA TTGGTACTTG GTTGGGAGGT GCTTGGCACT 360 TGGTTGGGAG GTACTTGGTG CCTGGTTGGG AGTAGTTGGT GTCCAGTTGA GAGGTGCTAG 420 GTGCTTGGTT GGGAGGTATT TGATTGGGAG GTGCTTGGCA TTTGGTTGGG AGGTACTTGG 480 TGCTTGGTTG GGAGATGCTG GGCCCTTGGT TGGGAGTAGT CTTTCCCATG CTCAGATCTG 540 AGCTGGCTTT GCCTGCATCA TCTCTGCGAG CCAACTGTCC CTGTTTGGCT CTGGCTTTTC 600 TTAACTATTT GAAATGGTTC CTTTACATGC TTGCCTCTGA ATTCTCTCCC AGAAGCCCTC 660 CCCAGGATCA CACCTGTGGC TGTTCACTCC CACCCCTGCC CCTGGGGCAA AGTTGACCTT 720 AGTGTTGATT CCTGGGCCTC TCCCCACACC TTCCCTTTGC TCCAGTCATT TGAATGAGAG 780 AGTGAAAACA GTGAGATGCC GGCTCCCACT CATCAGATCC AGTGATGCTG ATGACGCCAG 840 CCATGGTCCT ACCCTGAGGT GCTGACTCTG TCCCTGTAGG CTCCATGTCT CCGGAGAGGG 900 AGAGGGAGAG GGAGAGGATT CCAGCCTGTC ACAGCGCCCG CGGCAGCAAC CCCTGCTCGC 960 CAAATACTGA CTTGAATAGT GGTCCTCAGG CATAAGTGTG GGCGCTGAGT CCTGGGGCAG 1020 GACTGCTGTC CTGAGAGTGG GGACAGTGGA GGGTGGGTTT GTCCTCTGTC CTGGCCACAG 1080 GCACACGGTT GCGAGGAGCA TCTTGGCCTT CCTCCCGGCC CTGCTAGAGC CCCCGTCATC 1140 TCCTGTGCCC TCCTGCAGTG CTGTCCCCCA CCAGGGTCCT TCCTCAGAGG AGGGGGTTCC 1200 TGCCCCGGCC ATCATCAGGA AGGGGGTCTC TGGGTCCGAG CGTCCACCTC AGTGTGCACG 1260 TGGCCAAAAG GATCAAGAGC CCTGCAGCCA GGGGGGCCCC TCCTGAGACT CGACTTCGTT 1320 GCAGTTTCAG CAATGCAGGT GGCCCCGTGC GGACATCCAG GCAGGGTTGA GGGAAGGCAC 1380 ATCCCTCCCA GGCCCAGGGT ACCCATGTGG GTGGCAGAGC GGGCTCTGGG GATGACCCTC 1440 TGGCCCCTGA GGATCTGGGG CCAGAAAGAC ACTGGCTTAG CATGGGAGGA GTCCCCGGCC 1500 TGTACCAGCC TGACAAGGGG CTGCAGTGGC CCCCGGGTCT CAAATTAAAG CCAGGGTGAA 1560 ACCCAACCCC CTCTTTAAAA TGCAAAATGG CCCTTCCCTA AAATAACACA CAACCACAAC 1620 CGCAGCTGGC TCTGCACGAA GGCCATGCTG CAGCTCTTTT CTTCGGAAGT CGATTTTCCT 1680 CCGTGGAATT TGGCTGGGCT TGTGGTAGCG TTTGAGACTC TGCAAGAGCA CGTCCACGCC 1740 AACCAGTCTC TGGTCACCGA CTGGCTCGCA AATTCCCCAT TTAAGGAAAC CAGCAGGCCT 1800 CTGTTATGAA ACTCGGGGAA GGAATGTGAA TTATGCTCCA TGCGGAGGCT CCTGCTCCTG 1860 CACGTTTTCC AGCCTTTTCC ATGGGCCACG GTGGAGCATT TGGGGAAGGC CTGTGTGGAT 1920 TCCCCCCCAA GTCCAGACTG ATGCCCCTGA TACCTTCTCA GGAGGTGGCG GAGGGTCTGG 1980 GCTCTGTCCA GGCTCCTAGG GGTGGGGACG TGCAGGTAAA GCAAGGCGTC TGCCGCAGGC 2040 ACGCGGGAGC CTTCCCTGGG CTGGCTGCCA GCACCTTGGA GTCCCAGGCT GCCAGGAAAA 2100 GTTCACCCAC ACCCGGGCTT TGCTGGCGAA GGGTGAGTCA TATGATGGCC GGGCTCGGGC 2160 CCTCAGCAGA CACCAAGTGT GTTCCCAGAG CAGCCGCTCA GCGCCTGTAA CCTGGAACAG 2220 GCCAGCCTTT CGGGGCCTCA GTTTTCTCAT CTGCCTAATG GGAATAGCAA TTCCCACCTT 2280 CCCTTTGTTG GTTGGGTTCT CACTAGATGC ACAGGAGACA GCAGCTTGAG AGGGACTGTT 2340 TGGAGAGCTG TTCCATGTGA CACCCCTCTT ACCCTGTCCC CACGGGGCCG GAGGAGCAGG 2400 GGCTTGGTGA TAGCAGCTGG GCGCAGTCAG CCTCTGCAGG GAAGAGGGCA TGTTTGGTTC 2460 GAGGCTCCTA TGCCCTCATT CTTGTTGATC TTGTCACAGC CCCTCTGGAA GGTGGAGATG 2520 GTACTCGCTC AGGAACGATA CCACTCAAGG AAGCATGGCC CCCTGGATGG GGTGGCCCTT 2580 GGTGCACCTG AGGCTCCTGA GGCTGCAGAG CACCATGGTG GGGGAGGAGG CGGCTGTGTG 2640 TCTGTCATTT GCCTCTTCTG CTGAATGGAG ACCCCCAGAG GGCAAAGCGG GGCTTGTTCT 2700 CCCTGTGTCC CGGGATCACT CTCATGCCTG GCTTGGGCGA GCTGCCTGTT TCTAAATCAC 2760 TTGCTAAGGC TGAGGGGAAT GGGGTTTGCC GCCCACCCCA GGAAGAAGGG AGCAAGGGAG 2820 TCAGCACCAT TTTACAAGGA CCAAGAGTGG GAGGAGGCTC CTCAGAGGAC ATTCTGGGCA 2880 CTGTCCCCTT TCTCTGCTGT GAAGGGTGGA CAAAACACAA TAGGTCTGCC AGCCCTTGTG 2940 TCCTGTGGCT CATCCCAGCT GGCTGGGATG GGAACTGAGT CCTCCAAGCT GGTGTGGTTC 3000 CCCTCTGGTC TCCGCTGAGA GTCACGCCCA GCCTCTGGGC ACACACCCTG TGGTCACCTC 3060 CAAACAGGGC ACACTGGGCA CTGGTGGGGG TGGGACCTGC CATCCCAGAC CTGGTGTCTG 3120 CTCACTTTGT CTTGGTTCAT TGGCCAGAGA TCACGTAAGG GCGCCCTGAG GATGTGCTTG 3180 TTTCTCATGG ATGGGTGATG CTTGTCTCTT GGGAACATGG AGAAGCAAAG CCACGTCGCC 3240 CACAGACCTA CCCAGGAACA GCTGCAGCTG CAGGTTCAGG GTCCATCCCA GCCATGGGTT 3300 TTATTCTTTT TTTTTTGAGA CGGAGTGTTG CTGTCTCCCA 3340
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