Tag | Content |
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EnhancerAtlas ID | HS178-20846 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr6:159074380-159077500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr6:159075666-159075677 | GGATGACTCAG | + | 6.32 | Foxq1 | MA0040.1 | chr6:159074969-159074980 | AATAAACAATG | - | 6.02 | JUNB | MA0490.1 | chr6:159075666-159075677 | GGATGACTCAG | + | 6.14 | MYC | MA0147.3 | chr6:159075767-159075779 | GAGCACGTGGCT | - | 6.04 | SOX10 | MA0442.2 | chr6:159075965-159075976 | AAAACAAAGAC | + | 6.14 | TCF7L2 | MA0523.1 | chr6:159074899-159074913 | TTCCTTTGATCTGA | - | 6.17 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_02632 | chr6:159074789-159076958 | Astrocytes | SE_09522 | chr6:159073311-159077550 | CD14 | SE_15242 | chr6:159073751-159077595 | CD4_Memory_Primary_7pool | SE_16597 | chr6:159073338-159077176 | CD4_Naive_Primary_8pool | SE_17191 | chr6:159073720-159076873 | CD4p_CD225int_CD127p_Tmem | SE_17563 | chr6:159073699-159077653 | CD4p_CD25-_CD45RAp_Naive | SE_18193 | chr6:159073567-159077729 | CD4p_CD25-_CD45ROp_Memory | SE_18754 | chr6:159073254-159077363 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19401 | chr6:159073669-159077638 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20271 | chr6:159073414-159077584 | CD56 | SE_21839 | chr6:159073574-159076650 | CD8_Naive_7pool | SE_23027 | chr6:159073707-159077482 | CD8_primiary | SE_27252 | chr6:159073769-159074872 | Esophagus | SE_27252 | chr6:159074883-159076609 | Esophagus | SE_42870 | chr6:159074496-159077484 | Lung | SE_45067 | chr6:159074776-159077316 | NHLF | SE_45976 | chr6:159074538-159078465 | Osteoblasts | SE_49358 | chr6:159074392-159076385 | Right_Atrium | SE_50961 | chr6:159073750-159077293 | Sigmoid_Colon | SE_52770 | chr6:159073702-159077572 | Small_Intestine | SE_53918 | chr6:159073569-159077361 | Spleen | SE_62860 | chr6:159062856-159089459 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 6 | Chromosome | Start | End |
chr6 | 159074385 | 159076525 | chr6 | 159074587 | 159075256 | chr6 | 159075641 | 159075823 | chr6 | 159076608 | 159076855 | chr6 | 159075400 | 159076800 | chr6 | 159076335 | 159076366 |
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Enhancer Sequence | ATACAAAATT AGCGGAGGAT GGTGGTGCAT GCCTGTAATG TCAGCTACTC GGGAGGTTGA 60 GGCAGGAGAA TTTCATGAAC CTGGGAGGCG GAGGTTGTGG TGAGCCAAGA TCGCGCCATT 120 GCATTCCCGC CTGGGCAACA AGAGCGAACT CCGTCTCAGA GAAAAAAAAA AAGAATCTAT 180 GCAAGCAAAA AAGTCATGAG GTTTTCAGGT AAAATTTCAA GGACAATGCA GTCACTCAAC 240 TTTTCCCCTG TGTACGAGGC AGAAAGCATG GTGGCTGCAC GCTGAAGCTG TGAAACTTCT 300 CAAGGAAATA GCTGTGGTAA ACAATACAGG AGCGAGCTGC CGCCCGCTTG AAATGACCTG 360 CAGGGCTGTG GCTTGTGGGC TTTGAGAACG TTCTGTAGTC TTCCCTTGAA AGCGTGTGTG 420 GTGATGACAG TCACATTCAC ACGCACTCAT GCTACCGCAG ATCTCTGCAT TTCCACTCTG 480 GTGACGTTTC CCCCGTACCA GGGAGGGCTG AACATTTATT TCCTTTGATC TGATGACTGA 540 CTGCTCAGAG ACAATAGATG ATTGGATGAA AGAAATAGGG GCCCCTAAGA ATAAACAATG 600 TGTCCCTTTC CCATCCTCCT CATCTCTTTT CTTCATTGGT TTTACTTTTC TTGTACTTTT 660 CCCCTTTCAC CAGATTTAGA AGCCAAAGTC AAGATTTGCT GTTAGGCTGA GGAAAGCAAG 720 CAGGCATTGT TTCAAACTCC TAGTGCATGG CTGACTATTT CAGTCCCCTG GCGGAGCTGT 780 CCCACACGTC TCTCCCTGGG AAGCCCTCCC TGGTCCCACC AGCCCTCTCT GCTCCTGTGT 840 GGAGTGACTC TTGCCTTCTG ATCCTTGGGT TTTGTACTCA TCCCACCATG TTATGAGTTA 900 TTTGTCTGTG TGTCCATGTT CTGGCTGGGA TGGGTCCTTC TTAAATGCAG AGATTGAGTC 960 TCACTTCTTT TTAGATCCTC GATATCTGGC ACGTGCTTGA TACATAGAGG CCAATAAAAT 1020 CAGTGTTGAA CTGACACACT CAATGCCGTA ACCAAACTGT GTTTGTCTGG ATGCCGAAGT 1080 TCCACTGGGA TACAGCATGA CCAGATAAAG ACCAATGGAA ACACCTAGAT TGAAGTTTTC 1140 CCCATGGCTG CCCGCGTCCC TCCCAATCCC AGAACAGTGG CTTAACTTCC TACTCTTGGG 1200 CCTTCCTGAA GGGGAGATGG AAGGGTAGAA GAAACCCTTT TGAGTCGGGC TTGCTTTGTT 1260 CTGGCTGTTG CTCTAGGGCT GTGCCTGGAT GACTCAGTGA GTTCCCCAAA CAGCCCTGTG 1320 AAGCAGGGAT GGCTCCATGT CACGGAGGAG GAAGGCCAGT CTCCCAGAGA TGAAGCAGCT 1380 GGCCTGAGAG CACGTGGCTG AGTCCTGGCT GGGTATGAGC CCAGACTGTC TGGCTCCAAA 1440 AGTGACACAG AGACAGGATG GCTGAGTGTC GGGGGGGCTT CTCCACATGG CTGTAGGAGA 1500 ATGTTTCCTT CCAGGTGGTG CTGTGGTGTG GGATTTATTC ATTTTTAATT GCCAGATAAA 1560 ATCAGGCTGA TCGATGGAGT GCTGTAAAAC AAAGACAGGC ACCATTACAA AAATGTAGCA 1620 GGGGAGTTAG GAGACTGGAT CTAAGCTCCG AGCAGGTGAG GACGGTGCCT GACTCAGTGC 1680 TTGGGACATC ATAGAGCATT TAAGATCTTG TTGAGCAAAT GATGGAGTGA CCGAATAAAT 1740 GTCATCCTGG GAAAATGGAC CTAGGAGATT TCCGTATTCA AGCTATGAGA TTGTGAATTC 1800 CTGCGTGAGA TGATTAACAT ACAATTTCAA AGATTCCTGT TAAATTCCAA AATGACTCAG 1860 ATTTTTCTAT GCTTTTTGGA TTTCTGAAGA CTGAGGTTTT CTGCAGTGAG GACTCACTTG 1920 CCCCCTGCCC GTCCTTACTT CCTGCTGTAC TTGAATATGG GCTTCCTGCC CTAGGAAGGA 1980 AGTTTGACAT CGGAGTAAAT CTCCGTGTCG CAATATTCTT CAGGTTTCTC AATTCAAGCC 2040 AAACATCAAG TGCCTCCTGG CTGGGTGATG GGGGAATCGC TGAAATCTGA TATTGTCCCT 2100 AGAAGGCAAA CACTCAAGAC AGAATGAAAT CAGGGTCACC ATCGAAATAT ACAAATTAGA 2160 AAGCAGTTAA ATTTGAAGGA GCAATGGATC TTTATTGTAA ATGAGGAGAA AGTTTCTGAA 2220 CTGGGTAGCC TTGATCTGGC CCTTGAAGGG CTAATAGTAA GAGTGAGGCT GCTCTTACTG 2280 TTAGTACCAC GACTGTCAGC CGGCATTAGC TGAGTGTACT TATGAGCTGA GCACTGTGCT 2340 CTAGAGGTCT CCACATGCAT CAGCACGTTT CGTCATCATA GCACCGCCGT GAAGTGGGTG 2400 CTGCACCTGT CTACTTCGTA GATGAGGACA TGAAGCCCCA GAGGGCTTAA GTAACTTGCC 2460 CATCATCAGC TCAACAGCAA GTCGGTGGCA GAGGCAGCTA CTCACCCACA CAGCCAGCCC 2520 CCAGCCCTGG TCTCATGACT GTCCCCATCT CTTGCCTCAT TGGGCAGAAG GAAGAGTGGG 2580 GCCGATGCGT GGAAATGCAG AGCGCATGTG GTCAGGGAAT GGTCTTGAAT GAGGTCAGTA 2640 TGGGAGTGGC GAGCATTCTG TGGGAACTGA GGATGGAGGA GTCAGGAGAA CTGGATCGGG 2700 AGGTCACGAC TGGGATGCCT GTGCTTTAGA ATGTGTTTAC GGGAAGGGAA AACCAGCGTG 2760 ACTTCACTGG AGAGTGGAAG AGTGACACAT TCCCACCTCA GTATTGTCAC ATCTGCCGTC 2820 TCTCACCCTA GAGATGCCTT CTCCTCCTTT CCAATCCTCA CACAACTCCC CTCTTCTCCC 2880 AGGCCTGGCG GTGGCGTCTC AGCCAGGCAG GTGTCCTGTC CTTTCCTGTC ACCTGTCAGT 2940 CTTCCTCTTC CTCGTGGTCC ATTCAGCAAC ATCACTGCTG CTCTGGGTGG TTGCATGTGG 3000 TCGTTTGCCT GCAAGCAGGT GGGTGCAGCC AGTTCAGGAC CCCTGTGACA ACTATTCCTG 3060 TTACCTGCTT TGTGAGTGTT AAAAATGTCA TCCTTGGCCG GGTGCGATGG CTCACGCCTG 3120
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