Tag | Content |
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EnhancerAtlas ID | HS105-69140 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr6:43977340-43980620 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr6:43977381-43977399 | GGGAGGGAGGAAGGGAGA | + | 6.09 | EWSR1-FLI1 | MA0149.1 | chr6:43977393-43977411 | GGGAGAAGGGAAGGAGGG | + | 6.33 | EWSR1-FLI1 | MA0149.1 | chr6:43977389-43977407 | GGAAGGGAGAAGGGAAGG | + | 6.63 | EWSR1-FLI1 | MA0149.1 | chr6:43977420-43977438 | GGGAGGTAGGAAGGGAGG | + | 6.6 | EWSR1-FLI1 | MA0149.1 | chr6:43977424-43977442 | GGTAGGAAGGGAGGGAGG | + | 6.72 | EWSR1-FLI1 | MA0149.1 | chr6:43977358-43977376 | GGAGGGAAGGAGGGAGGG | + | 6.84 | EWSR1-FLI1 | MA0149.1 | chr6:43977465-43977483 | GGAAGGGGGGAAGAAAGG | + | 7.13 | EWSR1-FLI1 | MA0149.1 | chr6:43977473-43977491 | GGAAGAAAGGAAGAAAGA | + | 7.2 | EWSR1-FLI1 | MA0149.1 | chr6:43977346-43977364 | GGGAGGAGGGAAGGAGGG | + | 7.36 | EWSR1-FLI1 | MA0149.1 | chr6:43977377-43977395 | GAAAGGGAGGGAGGAAGG | + | 7.45 | EWSR1-FLI1 | MA0149.1 | chr6:43977350-43977368 | GGAGGGAAGGAGGGAAGG | + | 7.85 | EWSR1-FLI1 | MA0149.1 | chr6:43977354-43977372 | GGAAGGAGGGAAGGAGGG | + | 8.7 | FOSL2 | MA0478.1 | chr6:43979978-43979989 | GGATGACTCAG | + | 6.32 | JUNB | MA0490.1 | chr6:43979978-43979989 | GGATGACTCAG | + | 6.14 | RREB1 | MA0073.1 | chr6:43980328-43980348 | CCCCTACCCACCCCACCCAA | + | 6.06 | SPI1 | MA0080.4 | chr6:43979861-43979875 | AAGTTCCTCTTTTC | - | 6.08 | ZNF263 | MA0528.1 | chr6:43977406-43977427 | GAGGGAGGAAAGTGGGGAGGT | + | 6.03 | ZNF263 | MA0528.1 | chr6:43979730-43979751 | CCTTTCTAGCCTTCCTCCTCC | - | 6.06 | ZNF263 | MA0528.1 | chr6:43977421-43977442 | GGAGGTAGGAAGGGAGGGAGG | + | 6.11 | ZNF263 | MA0528.1 | chr6:43977379-43977400 | AAGGGAGGGAGGAAGGGAGAA | + | 6.28 | ZNF263 | MA0528.1 | chr6:43977446-43977467 | AGGGGAGGGGAAGGGAAAGGG | + | 6.33 | ZNF263 | MA0528.1 | chr6:43977470-43977491 | GGGGGAAGAAAGGAAGAAAGA | + | 6.3 | ZNF263 | MA0528.1 | chr6:43977359-43977380 | GAGGGAAGGAGGGAGGGAGAA | + | 6.45 | ZNF263 | MA0528.1 | chr6:43977374-43977395 | GGAGAAAGGGAGGGAGGAAGG | + | 6.66 | ZNF263 | MA0528.1 | chr6:43977402-43977423 | GAAGGAGGGAGGAAAGTGGGG | + | 6.77 | ZNF263 | MA0528.1 | chr6:43977386-43977407 | GGAGGAAGGGAGAAGGGAAGG | + | 6.89 | ZNF263 | MA0528.1 | chr6:43977383-43977404 | GAGGGAGGAAGGGAGAAGGGA | + | 6.8 | ZNF263 | MA0528.1 | chr6:43977387-43977408 | GAGGAAGGGAGAAGGGAAGGA | + | 6 | ZNF263 | MA0528.1 | chr6:43977344-43977365 | GAGGGAGGAGGGAAGGAGGGA | + | 7.07 | ZNF263 | MA0528.1 | chr6:43977371-43977392 | GAGGGAGAAAGGGAGGGAGGA | + | 7.11 | ZNF263 | MA0528.1 | chr6:43977351-43977372 | GAGGGAAGGAGGGAAGGAGGG | + | 7.1 | ZNF263 | MA0528.1 | chr6:43977394-43977415 | GGAGAAGGGAAGGAGGGAGGA | + | 7.23 | ZNF263 | MA0528.1 | chr6:43977434-43977455 | GAGGGAGGGCGGAGGGGAGGG | + | 7.27 | ZNF263 | MA0528.1 | chr6:43977363-43977384 | GAAGGAGGGAGGGAGAAAGGG | + | 7.45 | ZNF263 | MA0528.1 | chr6:43977367-43977388 | GAGGGAGGGAGAAAGGGAGGG | + | 7.49 | ZNF263 | MA0528.1 | chr6:43977355-43977376 | GAAGGAGGGAAGGAGGGAGGG | + | 8.14 | ZNF263 | MA0528.1 | chr6:43977340-43977361 | GAAGGAGGGAGGAGGGAAGGA | + | 8.17 | ZNF263 | MA0528.1 | chr6:43977347-43977368 | GGAGGAGGGAAGGAGGGAAGG | + | 8.35 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_33766 | chr6:43977031-43980823 | HCC1954 | SE_34623 | chr6:43977502-43980971 | HeLa | SE_41221 | chr6:43977275-43979991 | Left_Ventricle | SE_45608 | chr6:43977247-43981794 | Osteoblasts | SE_48994 | chr6:43977604-43979998 | Right_Atrium | SE_49741 | chr6:43977856-43979271 | Right_Ventricle | SE_51452 | chr6:43977692-43979722 | Skeletal_Muscle | SE_55652 | chr6:43967606-43993307 | u87 | SE_61323 | chr6:43961119-43979544 | HBL1 | SE_67450 | chr6:43967606-43993307 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr6 | 43979820 | 43980209 | chr6 | 43978439 | 43978901 | chr6 | 43977800 | 43980400 |
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| Number: 2 | ID | Chromosome | Start | End |
GH06I044008 | chr6 | 43975452 | 43977429 | GH06I044009 | chr6 | 43977606 | 43981134 |
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Enhancer Sequence | GAAGGAGGGA GGAGGGAAGG AGGGAAGGAG GGAGGGAGAA AGGGAGGGAG GAAGGGAGAA 60 GGGAAGGAGG GAGGAAAGTG GGGAGGTAGG AAGGGAGGGA GGGCGGAGGG GAGGGGAAGG 120 GAAAGGGAAG GGGGGAAGAA AGGAAGAAAG AGAGTTGAGC ATGCCTTGAA TGCTCTGAAG 180 GCTGCCATGC AAAGAAGGGT TAAACTGGTT CTCCAGGAGC AGAAGAAATG CCAGCAGAAG 240 GTGAACTCAG GGAGTCAGTT TTTAAATCAC CGACAGTAGG AAATCTTAAA AGTCAGATGG 300 TCACAATGTC GATTGGATGA TCCCAAAGGA CTACGAGCTT CTCAGGAATG AGTTTAAGCA 360 GAAGCAAAAG TAGCGCTTCA CAGAGGTGCT GTTGCTTCAA TGAAGGAACC AATGAATGGT 420 GAGTGAATTA ATGAATGAAT GAAACTACCA CTGAATACTA CAGAGAATTT CACATGCTGG 480 ACAGAAGACT GGAGACCTCT GACGTTTGTC TCAGAAGTGA GTCTGTGAGA CTGGCGCTAT 540 GCCAGACCCC AGGTAGGCAA CGAGCCATGG GCCCTGTCCT CAAAGAGCCC AGTGAGAGAT 600 GCACGCAGCA CACGCACAGA GGCAGAAAAC ACACTTTGAA TCTCTCTAGC AACCCCAGAC 660 AGGTCATGCT GGAAGACATT CATAGCAGTG CAAGGAGAAG CGTCTTGAGA GAAGCTCAGC 720 CCTGACTCCG CTCCCCATAC CTTCTCAGCT TTCTCAAGGA GGTAACTTTC TAGAACCCCC 780 TTTGGGCCAC TTTCCCAGGG GTGACCCTTT GGCACACGTC TGTCCTGAGG TCGTGGCCTG 840 TCTGGCAGCC TCCTCCTCAG GGTTAGGAGT GGGGTTGGCA CCTGGCCATC CTGCAGAGGG 900 CAGGGGTAGG TGCTTCAACA GCCCCAGCTC TGGGACATGT GCAGGTGCCC TAGTTCCAAG 960 CCCCCACTGG CAGGTTCAGA AGACTGAGAC ACATGGCCAG GCCCTGACCC CTTGCCTGCA 1020 AGCTTCCTAA GAGCAGGGAT CATCTCTTAC CTGCCTCGGT CTCTCAGTGC TGGCACAGCA 1080 TGGCTACTCA GTGTATGTGA GCTGAGTGGC AGAGTGCCAG GGCTGGCAGA GCTGCCATGA 1140 AAAGGGGTGC TGTGCTCAGG GAGATGGAGA TGGGGTGCCT TCCTAGTAGG GTGCAGTAGC 1200 ACTAGGCAGG GACTAGGAAG AGCATGCAAG TCCCCTGGGC CCCCTAAGGC CAGCACCGGG 1260 TCAGACTTGT CTTCTCTCCA TGTTCAGGGT CTGCCCTGTC TCCAGCAGCC CCACTGTGGC 1320 TGGTGACCTG TCAGTGACTC ACAGCCAGCT GTGGGCACAG AGTGGAGAAA GTGGCCTCCA 1380 GCTGAGCTCA TGCACTAGCA ATTAGCCCTC TACACCTCCT CACCATGGAG AGCCTCCCAG 1440 CTTCCACGCA CGCACGTCCC AGGCTGCCCT TTCCCAACCG CAGCGTGGCT CTTGTGCTTA 1500 TTTTAGCCTG ATGAAGCCTC TTGAAATGTC AGAGCTGCAA CCAACCAAGC TAGGGACCAT 1560 CCAGTTGAAT CCTTTCATTC AACCAGGGAG AAAATGGGGA TTCAGAGAGG GAGTGAGAGA 1620 TGCGCTTCAG GTCACACAGC TAATTGGTTG TGCAGCCAGA AATGAACTGC AGGCTTCCGG 1680 AGCCCAGATC CAGCTGTCCT TAACTCTAGG GGGCAATGTG CTTCAGGTAG CCCCTCACCA 1740 GACTTCTGGA GCCACTGGAG CCAGCACACA TGTGTTTGAA TCCTTCTTGG CCACTTGTCA 1800 GCTGTGAGAC TATGGGCAAG TTACTCAGCA TCTCCAGGCT TCTGTTTCTC CACCTGTAAA 1860 ATGAGGATAA CAGAGGCATG TCCCTCCCAG GTTGGTGTGA GGAATGAATG AGTTCATATA 1920 TCTGAACTGC TAAAAGCAGT GCCAAGCACA TAGCACACAC TCAAAACACA TTAGCTGACA 1980 TTGTGTAGTC ACCAAGACTT GGTCTCTGGT GTGGAAAGTT TAAAAATTCA GTTTTATGTG 2040 TTTGTCCATG GGTGAGCAGA TTCTGGGACA CCAGCCATAT AACCAGACTT CTGGAAAACT 2100 GGTGGTGCTA CTGTGGGGAC AGGTGTTGCT GTCAGAAAGA TCCACAGTAG ACACAGAAAC 2160 TGCCTTCCAC TTTGGCAGTC ACCATCTGAG ACCCACAGAT TGCAGACATC GAGGCAAAGG 2220 CAGTTTGGAG ATTCTCAGGG CTATTCAAGC TCGGTGAGCC TGAAGAAGTG CCCTTCTGAA 2280 CTCAAGAACT GGGCCTCTGT TTGTTAATCT GAAAAATAGG GGAAATCATA GCCTTGGGCT 2340 CACTGGGTGG TTGCAGGCAT TAGATCAGGT GGGACAGTAC CTGAAATAAT CCTTTCTAGC 2400 CTTCCTCCTC CCTCTTTCTT TGTCACGACC CCCATCATCT GCTTGAGGCC AGTTCTCTCG 2460 ATTCAGAGCT GCCTCCCCAC TGGGCCCAGT TGGATAAACA CTGACAAATT CTTCCCCTTC 2520 CAAGTTCCTC TTTTCCCAGT CACCAAATCT CTGATACCTC ACACCAGATG AGTTATGGTC 2580 CCAGAACATG TACAAGATTG GGGTGTTCTC ATTCCAACCC TGGAGATCCT TGTTGAATGG 2640 ATGACTCAGT GAATCAACAA CTGCAACGAT TCCCAGAACT TCCTGAAAAC TCACTCTGAG 2700 CTCTTAACAT TGGGCAACAC TCTGGTTTCC CCCAGAGCCC CACCACAAAC CACCTCTGAG 2760 GAGAGGCGGC TCTGCAGTTG CCTCATCACT CTTTGCTGCC CTTCATCATG CTCATTTACA 2820 CGAGAACTTT CTCTGCCCTT ACTTCTCCAC CACCCAGTCT GGACAACCAG GTGTGTTTGC 2880 ATTCTCCCCT GCAGGAGGGC AACACAACCG TTCTGCTGTC CATAACCACT GCTGGCATGC 2940 CTAGTGGTCA GTCTTGAGCC CTCTCCATCT GCCCAAGTCA CAACTGTCCC CCTACCCACC 3000 CCACCCAACT TCCTATGATT GCCTGCATAG GACAACTGAC TCTTCTTGCT TGCTATTCCA 3060 GCTCCACTAA TAGCCCATGA CCCCCTCTTA GCCCCAGCCA GCCCCACCTG TAGAGTCCTG 3120 CTACGAGTGA GCCATTCCTC CCCAGGGGCA TCACCTACTC GCTGCATTCT GTTCTTCAGG 3180 ACAGACTGGA GCTCCCCAGA CGAGAAGGCC TAAAGGGCTG GGAGCGGTGG CTCACTCCTG 3240 TAATCCCAGC ATTTTGGAGG CCAAGGCGGG TGGATCACCT 3280
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