Tag | Content |
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EnhancerAtlas ID | HS139-03546 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr1:160598940-160601610 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN | MA0488.1 | chr1:160601362-160601375 | AAAATGAGGTCAT | + | 6.2 | JUND(var.2) | MA0492.1 | chr1:160601361-160601376 | TAAAATGAGGTCATT | + | 6.36 | RUNX1 | MA0002.2 | chr1:160598981-160598992 | GTCTGTGGTTT | + | 6.62 | Sox6 | MA0515.1 | chr1:160599635-160599645 | CCATTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr1:160600486-160600507 | TCTTCCCCACTTCCCTGCCCC | - | 6.03 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_11148 | chr1:160598223-160603945 | CD20 | SE_11987 | chr1:160595919-160604487 | CD3 | SE_14605 | chr1:160597136-160605413 | CD4_Memory_Primary_7pool | SE_15558 | chr1:160597948-160600787 | CD4_Memory_Primary_8pool | SE_15558 | chr1:160601296-160602818 | CD4_Memory_Primary_8pool | SE_15991 | chr1:160597755-160600747 | CD4_Naive_Primary_7pool | SE_16559 | chr1:160597854-160600675 | CD4_Naive_Primary_8pool | SE_16992 | chr1:160597784-160602587 | CD4p_CD225int_CD127p_Tmem | SE_17490 | chr1:160595186-160605466 | CD4p_CD25-_CD45RAp_Naive | SE_17914 | chr1:160590964-160618183 | CD4p_CD25-_CD45ROp_Memory | SE_18278 | chr1:160590659-160619197 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19140 | chr1:160597781-160605501 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_25548 | chr1:160591270-160602519 | DND41 | SE_30951 | chr1:160591362-160605178 | Fetal_Thymus | SE_32518 | chr1:160599217-160600817 | GM12878 | SE_39629 | chr1:160597728-160604666 | Jurkat | SE_53267 | chr1:160598327-160600734 | Small_Intestine | SE_55114 | chr1:160598321-160601206 | Thymus | SE_55114 | chr1:160601299-160602522 | Thymus | SE_60518 | chr1:160576136-160655079 | DHL6 | SE_62055 | chr1:160575586-160612324 | Toledo | SE_62257 | chr1:160575404-160656474 | Tonsil | SE_66473 | chr1:160597728-160604666 | Jurkat |
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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: 1 | ID | Chromosome | Start | End |
GH01I160621 | chr1 | 160591446 | 160605374 |
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Enhancer Sequence | TGCTTTGCTC GAGTCTCCAC CCTGGGCCCT CTCCACCTAT TGTCTGTGGT TTAAACGTGA 60 TAACTTGGCA GACAGTCACA CATCCAAGGA AAAAGCCAGA GGGCGTTTTT TTTCTTGTCT 120 CTGAAAGTGT TGTCACAGAA ACACAGAAGC GTGTCTCTCT CTCTCTCTCT CTTCTCAAGT 180 CCCAAAATCT TATTATTAAT ATTTTTTTTA GGGAAGATGA AAAAGAAAAC TAAAAAGAAT 240 CTGAGAAACA AATGCAGTTC ACCTAGGAGA TACTGCGACG TTAGCGTAAC GGTGGGAGCG 300 TGCCGGATCT CCTTCCTGCC TTTCATGTGG TTCTGTCAGC AAAGGCTGCC ATCTTCAAGA 360 GATACATTCT TGTTCGTGGC AGTTTCCATT CAGAACTGGG GGTGGGGAAG GATCCTCATG 420 AACCATATAC TAATTTAAGT TCTGGGACCA TCCAAGTAAA CATTTTTACG GAGTTCACAG 480 CTTCCAGAAA AATCACTTAC AACCTGCCTA TCCCACCCAG CATTGCAGAG GCTACTAGCT 540 CCAGTGAGAT TGCGCTCATG CTTTCGTGGT AATACGAGTC TTTTCTGGGC ATGTAGCTGC 600 TCAGCTAGGA GCTATGTGTC TCAGCTTCCC TTATAGCGGG TGTGGCCCAT GACCAGGCTC 660 TGGGCTGTGC AAAGTTTCCA GGTTTTTCCT TTCCACCATT GTTTTTACGC TCGCTAAATT 720 GGGAAGACCC TAGAGAGAGA CCTGTCTTAG TGCCTGGAAC ATCTAAGTGA CTCTGAAACA 780 ATGGGAACTC CCTATTTGAA GAAATGACCT TGTTAGAAAG GGGAAGCCTC CGGAGCTCAC 840 TGGCAGGCGT CAGCCTTTTC TTTCACTGAG CTAACTCAGA GGTGCTGAGC CAGCGGTTTG 900 CTGATCTGCT GAAAAAGATC CTCTCTTCAA GATGAGCTTC CAGGGGCATT CCTTTCTAGA 960 TTCCTTCATT CTAGCACAGC CATATCTATT TCAGAATACA GTCATCGAGG ATGGCAGCAA 1020 GTCACACACT GTCCACAGCT GACCCACATC CACTGGCTTC ACATGACCTA GCCAGAGTAC 1080 TTCATAGCAC CCTAAGAATT GGACTTTGCA ATAAAGATGC TTCATTATGA TAGACATTAA 1140 CACACTGAAA TGGCAATTGG AACAAGGATG AATACATGAC CTGAACAAAT GTCACCTAAA 1200 GAAAAAGATT TCAAGGAACA TATAAGTTTT TGCACAGTTT CGCTTAAGTG AGTCCTGTCA 1260 AGATTCAGTG CTCACATCAC ATTGCATTCC GTCTCATCAC ACCATTAACC GCTGTGAGGT 1320 TTTCATTAAT GAAAATGAAA AATGTCTTAA AATCACTGTC CTGATGACAG ATGGCAAAGC 1380 AACCTCTAAT AAACCCTCGG ACCCCACCCT TTCATCCCAA GGCTGGGGTT TTCCTTTGTA 1440 TGCCCTAGGA AAAATGTCTT TGTTAACTGA CAGTTGCTGC TTTGGCTCGG GTCCCATCAT 1500 TTTGATGGAT GACTGCAATA ATGGCCCCCA GGAACTGGTT TCTCTTTCTT CCCCACTTCC 1560 CTGCCCCAGT CTGTTCTCTA TACTACTGGA GTTCCTCTTT GAAAAGCAAG ACTGATGGTG 1620 TCACTCCTCT ATCTAAAACT CTTTATTAGT TCCTATCACC TACAAGATAA TACAGAGCAA 1680 GACCCAGCTG TATCTGCTCC TCCCTCTGCC TGGAATGTCT TTCATCAGCT TGGGTAATTT 1740 CTACTTATTT TTAAAACCCA GTTTATGTCA CATTCTCTGG GATGCTCTCT CTAATCCCCC 1800 GAGACAGTGT TAATAATTCC CTCCTGTTTG TTGCCTTGCA TATATTTCCA TTTTACATCC 1860 GTCACACTGT CTAATCTCGG ATCATTGTTT ACTTATACAG CTGTCTTCTG CCTTAAGGCA 1920 AGGATCATGT CTTTTTTATC TTTGTGTACT GGCCCCTAGC ACAATGTAGA GTGTAAATGT 1980 TTTGTCAAAC TAAGTGCAGT GTTTTAAGAA CTGGTAGTAT TCGTTATTCA TGCGCAAACA 2040 CAAATCAAGG TACTGATACA ATTCTGTTTT CAGTATTTAG GCAATCTGGT ATACTGCGCA 2100 GGGCAGGCCA CAAACCAGCT GTGTGATCTG GTTCTGAGGC AGGGAAGGTC TGGTCCCCTA 2160 TCCCTGCAGG CTGGCAGGGT GGGGAGGAGG CATCTCTACT TTTATTACAT GTTGAATTGT 2220 GTTTTCCCAA ATTCATATGT TGATTTCCTT ATTTGGACAT AGCGTCTTCA CAGAGTTAAT 2280 TGAGTAAAAC TGAGGTCATT AGGGAGATGT TTTGGGCTGA ATTTTGTCTC CCCTCCCCCA 2340 AATTTCTATG TTGAAGCTCT AACCCCAAGG ACCTCAGAAT ATGACCGTAT TTGGAGGCAA 2400 GGTCTTTAAA GGTTATTAAG TTAAAATGAG GTCATTAGGG TGGCCCCTAA TCTAACCTAA 2460 CTGGTGTCCT TATAAGAAGA GGAAATCTGG ACACACAAAG AGACACCAGG AAAGAGAAAG 2520 AGAGAGAGAG AGAGATCAGG GTGTGAGTAC ACGAAGGAAA GACCAGGTGA GAACACAGTG 2580 AGAAGGTAGC CATATGCAAG CTAAGGCGAG AGGCCTCAGA AGACACCAAA CCTGCCAACA 2640 CCTTGACCTC AAACTTCTAG CCTCCAGAAC 2670
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