Tag | Content |
---|
EnhancerAtlas ID | HS046-06646 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr11:68119970-68123300 |
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 |
|
| 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 |
|
| 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I068352 | chr11 | 68119993 | 68123322 |
|
Enhancer Sequence | ATGTTGGTTG GGAAGTGCTC AGTGCTAGGT TGGGAGGTGA TCAGTCGGGA GGTGCTAGGT 60 GATTTGTTGG GAGGTGCATG ATGCTCAGTT GGGAGGTGCT AGGTGCTCGG TTGGAAGGTG 120 ATTGGTACTT TGTTAGGAGG TGCTTGGCGC TTGGTTGGGA GTTGTTGGTG TCCAGTTGAG 180 AGGTGCTAGG TGCTTGGTTG GGAGGTATTT GATTGGGAGG TGCTTGGCAC TTGGTTGGGA 240 GGTGCTCTGC ACTTGGTTGG GAGGTGCTCG GTGCTAGGTT GGGAGGTGAT CAGTTGGGAG 300 GTGCTAGATG CTCTGTTGGG AGGTGCATGA TGCTCAGTTG GGAGGTGCTA GGCGCTTGGT 360 TGGGAGGTAA TTGGTACTTG GTTGGGAGGT GCTTGGCACT TGGTTGGGAG GTACTTGGTG 420 CCTGGTTGGG AGTAGTTGGT GTCCAGTTGA GAGGTGCTAG GTGCTTGGTT GGGAGGTATT 480 TGATTGGGAG GTGCTTGGCA TTTGGTTGGG AGGTACTTGG TGCTTGGTTG GGAGATGCTG 540 GGCCCTTGGT TGGGAGTAGT CTTTCCCATG CTCAGATCTG AGCTGGCTTT GCCTGCATCA 600 TCTCTGCGAG CCAACTGTCC CTGTTTGGCT CTGGCTTTTC TTAACTATTT GAAATGGTTC 660 CTTTACATGC TTGCCTCTGA ATTCTCTCCC AGAAGCCCTC CCCAGGATCA CACCTGTGGC 720 TGTTCACTCC CACCCCTGCC CCTGGGGCAA AGTTGACCTT AGTGTTGATT CCTGGGCCTC 780 TCCCCACACC TTCCCTTTGC TCCAGTCATT TGAATGAGAG AGTGAAAACA GTGAGATGCC 840 GGCTCCCACT CATCAGATCC AGTGATGCTG ATGACGCCAG CCATGGTCCT ACCCTGAGGT 900 GCTGACTCTG TCCCTGTAGG CTCCATGTCT CCGGAGAGGG AGAGGGAGAG GGAGAGGATT 960 CCAGCCTGTC ACAGCGCCCG CGGCAGCAAC CCCTGCTCGC CAAATACTGA CTTGAATAGT 1020 GGTCCTCAGG CATAAGTGTG GGCGCTGAGT CCTGGGGCAG GACTGCTGTC CTGAGAGTGG 1080 GGACAGTGGA GGGTGGGTTT GTCCTCTGTC CTGGCCACAG GCACACGGTT GCGAGGAGCA 1140 TCTTGGCCTT CCTCCCGGCC CTGCTAGAGC CCCCGTCATC TCCTGTGCCC TCCTGCAGTG 1200 CTGTCCCCCA CCAGGGTCCT TCCTCAGAGG AGGGGGTTCC TGCCCCGGCC ATCATCAGGA 1260 AGGGGGTCTC TGGGTCCGAG CGTCCACCTC AGTGTGCACG TGGCCAAAAG GATCAAGAGC 1320 CCTGCAGCCA GGGGGGCCCC TCCTGAGACT CGACTTCGTT GCAGTTTCAG CAATGCAGGT 1380 GGCCCCGTGC GGACATCCAG GCAGGGTTGA GGGAAGGCAC ATCCCTCCCA GGCCCAGGGT 1440 ACCCATGTGG GTGGCAGAGC GGGCTCTGGG GATGACCCTC TGGCCCCTGA GGATCTGGGG 1500 CCAGAAAGAC ACTGGCTTAG CATGGGAGGA GTCCCCGGCC TGTACCAGCC TGACAAGGGG 1560 CTGCAGTGGC CCCCGGGTCT CAAATTAAAG CCAGGGTGAA ACCCAACCCC CTCTTTAAAA 1620 TGCAAAATGG CCCTTCCCTA AAATAACACA CAACCACAAC CGCAGCTGGC TCTGCACGAA 1680 GGCCATGCTG CAGCTCTTTT CTTCGGAAGT CGATTTTCCT CCGTGGAATT TGGCTGGGCT 1740 TGTGGTAGCG TTTGAGACTC TGCAAGAGCA CGTCCACGCC AACCAGTCTC TGGTCACCGA 1800 CTGGCTCGCA AATTCCCCAT TTAAGGAAAC CAGCAGGCCT CTGTTATGAA ACTCGGGGAA 1860 GGAATGTGAA TTATGCTCCA TGCGGAGGCT CCTGCTCCTG CACGTTTTCC AGCCTTTTCC 1920 ATGGGCCACG GTGGAGCATT TGGGGAAGGC CTGTGTGGAT TCCCCCCCAA GTCCAGACTG 1980 ATGCCCCTGA TACCTTCTCA GGAGGTGGCG GAGGGTCTGG GCTCTGTCCA GGCTCCTAGG 2040 GGTGGGGACG TGCAGGTAAA GCAAGGCGTC TGCCGCAGGC ACGCGGGAGC CTTCCCTGGG 2100 CTGGCTGCCA GCACCTTGGA GTCCCAGGCT GCCAGGAAAA GTTCACCCAC ACCCGGGCTT 2160 TGCTGGCGAA GGGTGAGTCA TATGATGGCC GGGCTCGGGC CCTCAGCAGA CACCAAGTGT 2220 GTTCCCAGAG CAGCCGCTCA GCGCCTGTAA CCTGGAACAG GCCAGCCTTT CGGGGCCTCA 2280 GTTTTCTCAT CTGCCTAATG GGAATAGCAA TTCCCACCTT CCCTTTGTTG GTTGGGTTCT 2340 CACTAGATGC ACAGGAGACA GCAGCTTGAG AGGGACTGTT TGGAGAGCTG TTCCATGTGA 2400 CACCCCTCTT ACCCTGTCCC CACGGGGCCG GAGGAGCAGG GGCTTGGTGA TAGCAGCTGG 2460 GCGCAGTCAG CCTCTGCAGG GAAGAGGGCA TGTTTGGTTC GAGGCTCCTA TGCCCTCATT 2520 CTTGTTGATC TTGTCACAGC CCCTCTGGAA GGTGGAGATG GTACTCGCTC AGGAACGATA 2580 CCACTCAAGG AAGCATGGCC CCCTGGATGG GGTGGCCCTT GGTGCACCTG AGGCTCCTGA 2640 GGCTGCAGAG CACCATGGTG GGGGAGGAGG CGGCTGTGTG TCTGTCATTT GCCTCTTCTG 2700 CTGAATGGAG ACCCCCAGAG GGCAAAGCGG GGCTTGTTCT CCCTGTGTCC CGGGATCACT 2760 CTCATGCCTG GCTTGGGCGA GCTGCCTGTT TCTAAATCAC TTGCTAAGGC TGAGGGGAAT 2820 GGGGTTTGCC GCCCACCCCA GGAAGAAGGG AGCAAGGGAG TCAGCACCAT TTTACAAGGA 2880 CCAAGAGTGG GAGGAGGCTC CTCAGAGGAC ATTCTGGGCA CTGTCCCCTT TCTCTGCTGT 2940 GAAGGGTGGA CAAAACACAA TAGGTCTGCC AGCCCTTGTG TCCTGTGGCT CATCCCAGCT 3000 GGCTGGGATG GGAACTGAGT CCTCCAAGCT GGTGTGGTTC CCCTCTGGTC TCCGCTGAGA 3060 GTCACGCCCA GCCTCTGGGC ACACACCCTG TGGTCACCTC CAAACAGGGC ACACTGGGCA 3120 CTGGTGGGGG TGGGACCTGC CATCCCAGAC CTGGTGTCTG CTCACTTTGT CTTGGTTCAT 3180 TGGCCAGAGA TCACGTAAGG GCGCCCTGAG GATGTGCTTG TTTCTCATGG ATGGGTGATG 3240 CTTGTCTCTT GGGAACATGG AGAAGCAAAG CCACGTCGCC CACAGACCTA CCCAGGAACA 3300 GCTGCAGCTG CAGGTTCAGG GTCCATCCCA 3330
|