Tag | Content |
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EnhancerAtlas ID | HS003-03356 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr1:203556970-203559680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:203557521-203557539 | CTTTCCTTCCTTCCTTCC | - | 10.53 | EWSR1-FLI1 | MA0149.1 | chr1:203558132-203558150 | GGAGGGAGGGAAGGATGA | + | 6.33 | EWSR1-FLI1 | MA0149.1 | chr1:203557505-203557523 | CCTTCTTTCCTTCTTTCT | - | 6.55 | EWSR1-FLI1 | MA0149.1 | chr1:203557533-203557551 | CCTTCCTTCTTTCTTTCT | - | 6.56 | EWSR1-FLI1 | MA0149.1 | chr1:203557485-203557503 | CTTTCCTTCTTTCCTTCT | - | 6.95 | EWSR1-FLI1 | MA0149.1 | chr1:203557493-203557511 | CTTTCCTTCTTTCCTTCT | - | 6.95 | EWSR1-FLI1 | MA0149.1 | chr1:203557501-203557519 | CTTTCCTTCTTTCCTTCT | - | 6.95 | EWSR1-FLI1 | MA0149.1 | chr1:203557481-203557499 | CTTTCTTTCCTTCTTTCC | - | 7.22 | EWSR1-FLI1 | MA0149.1 | chr1:203557509-203557527 | CTTTCCTTCTTTCTTTCC | - | 7.24 | EWSR1-FLI1 | MA0149.1 | chr1:203557513-203557531 | CCTTCTTTCTTTCCTTCC | - | 7.69 | EWSR1-FLI1 | MA0149.1 | chr1:203557489-203557507 | CCTTCTTTCCTTCTTTCC | - | 7.85 | EWSR1-FLI1 | MA0149.1 | chr1:203557497-203557515 | CCTTCTTTCCTTCTTTCC | - | 7.85 | EWSR1-FLI1 | MA0149.1 | chr1:203557529-203557547 | CCTTCCTTCCTTCTTTCT | - | 7.85 | EWSR1-FLI1 | MA0149.1 | chr1:203557517-203557535 | CTTTCTTTCCTTCCTTCC | - | 8.46 | EWSR1-FLI1 | MA0149.1 | chr1:203557525-203557543 | CCTTCCTTCCTTCCTTCT | - | 9.09 | Nr2f6(var.2) | MA0728.1 | chr1:203557777-203557792 | TGAACTCCTGACCTT | - | 6.04 | Stat6 | MA0520.1 | chr1:203558905-203558920 | TTTTCCCAGGAAATG | - | 6.04 | Stat6 | MA0520.1 | chr1:203558214-203558229 | GTTTCTCTGGAAAAA | - | 6.35 | ZNF263 | MA0528.1 | chr1:203557517-203557538 | CTTTCTTTCCTTCCTTCCTTC | - | 6.03 | ZNF263 | MA0528.1 | chr1:203557513-203557534 | CCTTCTTTCTTTCCTTCCTTC | - | 6.44 | ZNF263 | MA0528.1 | chr1:203557521-203557542 | CTTTCCTTCCTTCCTTCCTTC | - | 6.48 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 203558276 | 203558728 | chr1 | 203558936 | 203559028 | chr1 | 203558400 | 203558576 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I203589 | chr1 | 203558318 | 203563609 |
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Enhancer Sequence | TTTTGCTCTA TGCTCACTCC TAACCTTCCT GGTGGCCCAG GGACTTCTGG CAGAAAACAA 60 GTTTCCTAAT CAGCCAAAAG CATGTACAAC ACCTGAAGAG AGGACAGGAT ACATGGTCCT 120 CAGCAGGCTT CATGTTTGGG AGACACCACG CCTTCTCTCA GGAAAGTTCC AGTCTGAAAG 180 GGTGAACAGG TACAGAGAAG GATACATTCA CAAAACGAAA CAATAATAGC ACGAAGACCC 240 AGAAATGGCA AATAAAAACA TGGTAACACT TCCTCTTCCA TGGAGAATGT ACAGAATCGT 300 GACAGAGGAC AAAATGCAGA GACAGTCACA GAAATAAGTA CCCAGTCCTG CTCCCCTTGC 360 CAGCACTGCT CCTGGGCCAT CAATTCCCCA CTCTGTGGGG TTTAACAGCT AAGAACCCAC 420 TGATACTGAT CCCCTGGGCC ACAGTTCTTC TCCTCCAAAG CAGCAGATGA AAAATTCATG 480 GTGACAGCTT CAGGCCTCCA AATGCTGCTT GCTTTCTTTC CTTCTTTCCT TCTTTCCTTC 540 TTTCCTTCTT TCTTTCCTTC CTTCCTTCCT TCTTTCTTTC TTCTTTTTTT TTTTTTTTTT 600 TTTTTTTTTG GTGGAGTCTT GCTCTGTCCC CCTGGCTGGA GTGCAATGGT GCCATCTCGG 660 CTCACTGCAA CCTCTGCCTC CCAGGTTCAA AAGATTCTCC TGCCTTAACG TCCTAAGTAG 720 CTGGGGTTAC AGGTGCCTGC CACCACGCCC AGCTATTTTT TTATATTTAG TAGAGATGGG 780 GTTTCACCTT TTTGGCCAGG CTGGTCTTGA ACTCCTGACC TTAGGTGATC CGCCCACCTC 840 AGCCTCCCAA AGTGCTGGGA TTATAGGTGT TAGCCACTGC ACCCAACCCA TTTGCTGCTT 900 TCCGAGGCTG CTGTCTGCAG AGAACCAAGG ACCACCAGGA AGGCAATGGG CCAGAACTTT 960 GGCCCAGGCC ATCTTCTCAT CCAGAGCAGA TAAGTCCTTT CTGAGAGAGA CAGAGGAGGA 1020 GACACAGCCA GTGACCTGGG ATGCTAGGTG TTGGTTTGCC AGCTTGCTAT AGGATGTGAC 1080 CCCTTCATTC CCATTCCAAA GTGCTTAAAG GGACCCGAAG GTCCATCCTG TTCTGTCCAC 1140 CCCAGCCCAG GTTGCTGCAA TAGGAGGGAG GGAAGGATGA GAAGACAAGG ATGGCAGGGA 1200 AGTGGGGAAG GGGCAAACCT GGCAATTCCA GCTTTAGCTA CTGAGTTTCT CTGGAAAAAG 1260 AAAATTTCAT GTGAAAGCAA GGGCATCATT GGATGTAAGG AGTTCTCTGC TATGTCATCA 1320 CTCTATCCAC AGCACCCAGC ACAAAGGAAG CTTTTTAAAA ATGCATGCTG CATGAGCATC 1380 AGTGAATTAA TCCCTAAACA ACTGTCCATC CTTTTTTCCA TCCTCTCCTG CAGGCCCAGC 1440 TGTCCCCAGC CTAGTCAGAG AGGAGAAAGG ACTTTATCCT GATCCACTCT GGGCCTGGAG 1500 CTCTCTGTAG CCAATTTGTG GCATTACTGA GGAGAAAGAT GCATTTGGGA TCAGCCCACA 1560 TCCCAGCCCC TGCTCGGCAG GAGGGCTGAT GGGGCCTCAG GCTGTGAAAG AGAAAGTCTG 1620 AAAATGGCAG AAAGAGGCTG TTAATAAAAA CAGGAGGGGT GTGGCTCAGG GGCTTGTGTA 1680 CATAACACAT TCATTCATGC AGATTCACAA AAGCCCATCT TTTTTCAGAT ACGAAGATAC 1740 ACACTCATAA AAGCAGAGAC GCACTTTAAG ATCCTGATAT GTGTTTCCTC CCTACCTTAT 1800 CCCCAACATA TATAATAAAG TCATGAAATC ACACAATACC TTCCAACCTT GCTCTCCCTC 1860 CCACAGAGTG GAGTTCTCCC AGAAAGCAAT GTAGCCTGGG CCCAGAGCTT GGGGAGTAAC 1920 TAACACCATT TGCATTTTTC CCAGGAAATG GGAAGAGCTG GTGTGGCATG TGGCAGCCCA 1980 AGCCCTCACA CATCCCACTG ACTGACATTT TGACATCCTT GAATTTGGCC GGGCTGCTCT 2040 GCGGAGACAA ATCTTCCCCC TGTCCCTTCC CAGACAATCT CACTTCATTC TGACGGCTCT 2100 TGGCCCTAGC CTGTCAAACT AGGTCCTTGG TCCCTGAACA CAGCACAACA TGGGTACCTT 2160 CACACTAGCC CCGCTTCAAG AGGAACCAGA TCACTCTTCT CTGTCTCAGT ACTCTCCCAA 2220 CACCAGCCCC CCACCGCTTC TCTTTTTAAG AGACAGGAAG GGCTGGGCAC GGTGGCTTGC 2280 ACCTGTAATC CCAGCACTTT GGGAGGTCTC AGTGGGTGGA TTACAAGGTC AGGAGTTCGA 2340 GACCAGCCTG GCCAAGATGG TGAAACCCCG TCTTTACTTA AAAAAAAATA TACAAAAAAT 2400 ATTAGCTGGG CGTGGTGGCG CATGCTATAA TCCCAGCTAC TCAGGAGGCT GAGGCAGGAG 2460 AATTGCTTGA ACCTGGGAGG CAGAGGTTGC AGTGAGCCAC TATCGCCCCA CTATACTCCA 2520 GCCTGGGTGA CAGAGCGAGA CTCCGTCTCA AAAAAAAAAG AGACAGGATC TTGCTCTGTT 2580 GCCCAGGCTG GAGTGCAGTG GTGAGATCAC AGCTCACTGC AGCCTCAACC TCCTGGGCTC 2640 AAGAAATCCT CCCACCTCAG CCTCCCATGT AGCTCGGACT AGAGGTGCAT GCCACCATGC 2700 CTGGCTAACC 2710
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