Tag | Content |
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EnhancerAtlas ID | HS133-02678 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:160599330-160602420 |
Target genes | Number: 15 | Name | Ensembl ID |
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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 | 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: 24 | 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_53267 | chr1:160601595-160602466 | 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 | CAGAACTGGG GGTGGGGAAG GATCCTCATG AACCATATAC TAATTTAAGT TCTGGGACCA 60 TCCAAGTAAA CATTTTTACG GAGTTCACAG CTTCCAGAAA AATCACTTAC AACCTGCCTA 120 TCCCACCCAG CATTGCAGAG GCTACTAGCT CCAGTGAGAT TGCGCTCATG CTTTCGTGGT 180 AATACGAGTC TTTTCTGGGC ATGTAGCTGC TCAGCTAGGA GCTATGTGTC TCAGCTTCCC 240 TTATAGCGGG TGTGGCCCAT GACCAGGCTC TGGGCTGTGC AAAGTTTCCA GGTTTTTCCT 300 TTCCACCATT GTTTTTACGC TCGCTAAATT GGGAAGACCC TAGAGAGAGA CCTGTCTTAG 360 TGCCTGGAAC ATCTAAGTGA CTCTGAAACA ATGGGAACTC CCTATTTGAA GAAATGACCT 420 TGTTAGAAAG GGGAAGCCTC CGGAGCTCAC TGGCAGGCGT CAGCCTTTTC TTTCACTGAG 480 CTAACTCAGA GGTGCTGAGC CAGCGGTTTG CTGATCTGCT GAAAAAGATC CTCTCTTCAA 540 GATGAGCTTC CAGGGGCATT CCTTTCTAGA TTCCTTCATT CTAGCACAGC CATATCTATT 600 TCAGAATACA GTCATCGAGG ATGGCAGCAA GTCACACACT GTCCACAGCT GACCCACATC 660 CACTGGCTTC ACATGACCTA GCCAGAGTAC TTCATAGCAC CCTAAGAATT GGACTTTGCA 720 ATAAAGATGC TTCATTATGA TAGACATTAA CACACTGAAA TGGCAATTGG AACAAGGATG 780 AATACATGAC CTGAACAAAT GTCACCTAAA GAAAAAGATT TCAAGGAACA TATAAGTTTT 840 TGCACAGTTT CGCTTAAGTG AGTCCTGTCA AGATTCAGTG CTCACATCAC ATTGCATTCC 900 GTCTCATCAC ACCATTAACC GCTGTGAGGT TTTCATTAAT GAAAATGAAA AATGTCTTAA 960 AATCACTGTC CTGATGACAG ATGGCAAAGC AACCTCTAAT AAACCCTCGG ACCCCACCCT 1020 TTCATCCCAA GGCTGGGGTT TTCCTTTGTA TGCCCTAGGA AAAATGTCTT TGTTAACTGA 1080 CAGTTGCTGC TTTGGCTCGG GTCCCATCAT TTTGATGGAT GACTGCAATA ATGGCCCCCA 1140 GGAACTGGTT TCTCTTTCTT CCCCACTTCC CTGCCCCAGT CTGTTCTCTA TACTACTGGA 1200 GTTCCTCTTT GAAAAGCAAG ACTGATGGTG TCACTCCTCT ATCTAAAACT CTTTATTAGT 1260 TCCTATCACC TACAAGATAA TACAGAGCAA GACCCAGCTG TATCTGCTCC TCCCTCTGCC 1320 TGGAATGTCT TTCATCAGCT TGGGTAATTT CTACTTATTT TTAAAACCCA GTTTATGTCA 1380 CATTCTCTGG GATGCTCTCT CTAATCCCCC GAGACAGTGT TAATAATTCC CTCCTGTTTG 1440 TTGCCTTGCA TATATTTCCA TTTTACATCC GTCACACTGT CTAATCTCGG ATCATTGTTT 1500 ACTTATACAG CTGTCTTCTG CCTTAAGGCA AGGATCATGT CTTTTTTATC TTTGTGTACT 1560 GGCCCCTAGC ACAATGTAGA GTGTAAATGT TTTGTCAAAC TAAGTGCAGT GTTTTAAGAA 1620 CTGGTAGTAT TCGTTATTCA TGCGCAAACA CAAATCAAGG TACTGATACA ATTCTGTTTT 1680 CAGTATTTAG GCAATCTGGT ATACTGCGCA GGGCAGGCCA CAAACCAGCT GTGTGATCTG 1740 GTTCTGAGGC AGGGAAGGTC TGGTCCCCTA TCCCTGCAGG CTGGCAGGGT GGGGAGGAGG 1800 CATCTCTACT TTTATTACAT GTTGAATTGT GTTTTCCCAA ATTCATATGT TGATTTCCTT 1860 ATTTGGACAT AGCGTCTTCA CAGAGTTAAT TGAGTAAAAC TGAGGTCATT AGGGAGATGT 1920 TTTGGGCTGA ATTTTGTCTC CCCTCCCCCA AATTTCTATG TTGAAGCTCT AACCCCAAGG 1980 ACCTCAGAAT ATGACCGTAT TTGGAGGCAA GGTCTTTAAA GGTTATTAAG TTAAAATGAG 2040 GTCATTAGGG TGGCCCCTAA TCTAACCTAA CTGGTGTCCT TATAAGAAGA GGAAATCTGG 2100 ACACACAAAG AGACACCAGG AAAGAGAAAG AGAGAGAGAG AGAGATCAGG GTGTGAGTAC 2160 ACGAAGGAAA GACCAGGTGA GAACACAGTG AGAAGGTAGC CATATGCAAG CTAAGGCGAG 2220 AGGCCTCAGA AGACACCAAA CCTGCCAACA CCTTGACCTC AAACTTCTAG CCTCCAGAAC 2280 CAGGAGAAAA ATAAATTTCT GTTATTTAAA CCACCCAATC TGTTGTACTT TATTATGGCA 2340 GCCCTAGCAA ACTGAGACAG GTGGGCCCTA ATCCAATATG ACTGTTGTCC TTATGAGAAG 2400 AGGAAATTTG GACACAGAAA TACACATAGA GAGAAGATGA TATGAAGAGA CAAGGAGAAG 2460 ACAGCCATTT ACAAGCCAGG GAGAGGCGCC TGGGAGAGAT CCTTCTCTGA CAGCCCTCAG 2520 AGAAGAACAA TCCTGCTGAC ACCTTGACTT TAGACTTCTA GCCTCCAGAA CTGAGAGCCA 2580 ATACATTTTG ATTGTTTAAG CCACTCAGTG TGTGGTCCTT TGTTACAGCA GCCTTAGCAA 2640 ACTCATACAC AGTGGCAAGC CTCTATTGGC AGTTCTTATT GACACACACA CACACTGAAT 2700 CAAGGACTGT CTACTCTGGG AGGGACTTCA TTTGTTCGCC CTTTTCATTT TACTGGGGAT 2760 GAAACAGAGA CCCAAGAGAG GGGAACGGCT GGACAGTTCT CTTACAAACC GAGCCGAGAT 2820 CCTGACAGGG CCCTTCCTGT GGTGCCAGGT TTCTACTGCT TCCTGTCCCT CCACTCCTCA 2880 CAAGAACCAG CTTCCTACTC AGTAAATCTG GTTCCCACTG GTGCATTCTT GGTCCTCAGA 2940 GTGGCTTAGA TGGGTAAGTC CATCTTCACA TGTTTTCTTA GAACGTCCTG AGCTGAGTGC 3000 CCTTAGTATA AGCTTTATGG CCCACCAACA CTTTGGTATG CCCTAATTAA ATTCTTTTTA 3060 AACTACATTG AGGAGCATGA AGAAAGTTCT 3090
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