Tag | Content |
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EnhancerAtlas ID | HS098-10465 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:68120050-68123400 |
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 | ATGCTCAGTT GGGAGGTGCT AGGTGCTCGG TTGGAAGGTG ATTGGTACTT TGTTAGGAGG 60 TGCTTGGCGC TTGGTTGGGA GTTGTTGGTG TCCAGTTGAG AGGTGCTAGG TGCTTGGTTG 120 GGAGGTATTT GATTGGGAGG TGCTTGGCAC TTGGTTGGGA GGTGCTCTGC ACTTGGTTGG 180 GAGGTGCTCG GTGCTAGGTT GGGAGGTGAT CAGTTGGGAG GTGCTAGATG CTCTGTTGGG 240 AGGTGCATGA TGCTCAGTTG GGAGGTGCTA GGCGCTTGGT TGGGAGGTAA TTGGTACTTG 300 GTTGGGAGGT GCTTGGCACT TGGTTGGGAG GTACTTGGTG CCTGGTTGGG AGTAGTTGGT 360 GTCCAGTTGA GAGGTGCTAG GTGCTTGGTT GGGAGGTATT TGATTGGGAG GTGCTTGGCA 420 TTTGGTTGGG AGGTACTTGG TGCTTGGTTG GGAGATGCTG GGCCCTTGGT TGGGAGTAGT 480 CTTTCCCATG CTCAGATCTG AGCTGGCTTT GCCTGCATCA TCTCTGCGAG CCAACTGTCC 540 CTGTTTGGCT CTGGCTTTTC TTAACTATTT GAAATGGTTC CTTTACATGC TTGCCTCTGA 600 ATTCTCTCCC AGAAGCCCTC CCCAGGATCA CACCTGTGGC TGTTCACTCC CACCCCTGCC 660 CCTGGGGCAA AGTTGACCTT AGTGTTGATT CCTGGGCCTC TCCCCACACC TTCCCTTTGC 720 TCCAGTCATT TGAATGAGAG AGTGAAAACA GTGAGATGCC GGCTCCCACT CATCAGATCC 780 AGTGATGCTG ATGACGCCAG CCATGGTCCT ACCCTGAGGT GCTGACTCTG TCCCTGTAGG 840 CTCCATGTCT CCGGAGAGGG AGAGGGAGAG GGAGAGGATT CCAGCCTGTC ACAGCGCCCG 900 CGGCAGCAAC CCCTGCTCGC CAAATACTGA CTTGAATAGT GGTCCTCAGG CATAAGTGTG 960 GGCGCTGAGT CCTGGGGCAG GACTGCTGTC CTGAGAGTGG GGACAGTGGA GGGTGGGTTT 1020 GTCCTCTGTC CTGGCCACAG GCACACGGTT GCGAGGAGCA TCTTGGCCTT CCTCCCGGCC 1080 CTGCTAGAGC CCCCGTCATC TCCTGTGCCC TCCTGCAGTG CTGTCCCCCA CCAGGGTCCT 1140 TCCTCAGAGG AGGGGGTTCC TGCCCCGGCC ATCATCAGGA AGGGGGTCTC TGGGTCCGAG 1200 CGTCCACCTC AGTGTGCACG TGGCCAAAAG GATCAAGAGC CCTGCAGCCA GGGGGGCCCC 1260 TCCTGAGACT CGACTTCGTT GCAGTTTCAG CAATGCAGGT GGCCCCGTGC GGACATCCAG 1320 GCAGGGTTGA GGGAAGGCAC ATCCCTCCCA GGCCCAGGGT ACCCATGTGG GTGGCAGAGC 1380 GGGCTCTGGG GATGACCCTC TGGCCCCTGA GGATCTGGGG CCAGAAAGAC ACTGGCTTAG 1440 CATGGGAGGA GTCCCCGGCC TGTACCAGCC TGACAAGGGG CTGCAGTGGC CCCCGGGTCT 1500 CAAATTAAAG CCAGGGTGAA ACCCAACCCC CTCTTTAAAA TGCAAAATGG CCCTTCCCTA 1560 AAATAACACA CAACCACAAC CGCAGCTGGC TCTGCACGAA GGCCATGCTG CAGCTCTTTT 1620 CTTCGGAAGT CGATTTTCCT CCGTGGAATT TGGCTGGGCT TGTGGTAGCG TTTGAGACTC 1680 TGCAAGAGCA CGTCCACGCC AACCAGTCTC TGGTCACCGA CTGGCTCGCA AATTCCCCAT 1740 TTAAGGAAAC CAGCAGGCCT CTGTTATGAA ACTCGGGGAA GGAATGTGAA TTATGCTCCA 1800 TGCGGAGGCT CCTGCTCCTG CACGTTTTCC AGCCTTTTCC ATGGGCCACG GTGGAGCATT 1860 TGGGGAAGGC CTGTGTGGAT TCCCCCCCAA GTCCAGACTG ATGCCCCTGA TACCTTCTCA 1920 GGAGGTGGCG GAGGGTCTGG GCTCTGTCCA GGCTCCTAGG GGTGGGGACG TGCAGGTAAA 1980 GCAAGGCGTC TGCCGCAGGC ACGCGGGAGC CTTCCCTGGG CTGGCTGCCA GCACCTTGGA 2040 GTCCCAGGCT GCCAGGAAAA GTTCACCCAC ACCCGGGCTT TGCTGGCGAA GGGTGAGTCA 2100 TATGATGGCC GGGCTCGGGC CCTCAGCAGA CACCAAGTGT GTTCCCAGAG CAGCCGCTCA 2160 GCGCCTGTAA CCTGGAACAG GCCAGCCTTT CGGGGCCTCA GTTTTCTCAT CTGCCTAATG 2220 GGAATAGCAA TTCCCACCTT CCCTTTGTTG GTTGGGTTCT CACTAGATGC ACAGGAGACA 2280 GCAGCTTGAG AGGGACTGTT TGGAGAGCTG TTCCATGTGA CACCCCTCTT ACCCTGTCCC 2340 CACGGGGCCG GAGGAGCAGG GGCTTGGTGA TAGCAGCTGG GCGCAGTCAG CCTCTGCAGG 2400 GAAGAGGGCA TGTTTGGTTC GAGGCTCCTA TGCCCTCATT CTTGTTGATC TTGTCACAGC 2460 CCCTCTGGAA GGTGGAGATG GTACTCGCTC AGGAACGATA CCACTCAAGG AAGCATGGCC 2520 CCCTGGATGG GGTGGCCCTT GGTGCACCTG AGGCTCCTGA GGCTGCAGAG CACCATGGTG 2580 GGGGAGGAGG CGGCTGTGTG TCTGTCATTT GCCTCTTCTG CTGAATGGAG ACCCCCAGAG 2640 GGCAAAGCGG GGCTTGTTCT CCCTGTGTCC CGGGATCACT CTCATGCCTG GCTTGGGCGA 2700 GCTGCCTGTT TCTAAATCAC TTGCTAAGGC TGAGGGGAAT GGGGTTTGCC GCCCACCCCA 2760 GGAAGAAGGG AGCAAGGGAG TCAGCACCAT TTTACAAGGA CCAAGAGTGG GAGGAGGCTC 2820 CTCAGAGGAC ATTCTGGGCA CTGTCCCCTT TCTCTGCTGT GAAGGGTGGA CAAAACACAA 2880 TAGGTCTGCC AGCCCTTGTG TCCTGTGGCT CATCCCAGCT GGCTGGGATG GGAACTGAGT 2940 CCTCCAAGCT GGTGTGGTTC CCCTCTGGTC TCCGCTGAGA GTCACGCCCA GCCTCTGGGC 3000 ACACACCCTG TGGTCACCTC CAAACAGGGC ACACTGGGCA CTGGTGGGGG TGGGACCTGC 3060 CATCCCAGAC CTGGTGTCTG CTCACTTTGT CTTGGTTCAT TGGCCAGAGA TCACGTAAGG 3120 GCGCCCTGAG GATGTGCTTG TTTCTCATGG ATGGGTGATG CTTGTCTCTT GGGAACATGG 3180 AGAAGCAAAG CCACGTCGCC CACAGACCTA CCCAGGAACA GCTGCAGCTG CAGGTTCAGG 3240 GTCCATCCCA GCCATGGGTT TTATTCTTTT TTTTTTGAGA CGGAGTGTTG CTGTCTCCCA 3300 GGCTGAGAGT GCAGTGGTGT GATCTTGGCT CACTGCAAGC TCCGCCTCCC 3350
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