Tag | Content |
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EnhancerAtlas ID | HS184-13532 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:39940270-39942830 |
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 | chr17:39941248-39941266 | GGGAGCAGGGAAGGCAGG | + | 6.16 | ZNF263 | MA0528.1 | chr17:39941249-39941270 | GGAGCAGGGAAGGCAGGGGGC | + | 6.05 | ZNF263 | MA0528.1 | chr17:39940642-39940663 | TTCTCCTCCTCCCCCGCATCC | - | 6.42 | ZNF263 | MA0528.1 | chr17:39942365-39942386 | GGGGGAGTAGGGAGGGAGGGA | + | 6.54 | ZNF263 | MA0528.1 | chr17:39941655-39941676 | GAGGCAGGAAGAGAAGGAAGA | + | 7.1 | ZNF263 | MA0528.1 | chr17:39940645-39940666 | TCCTCCTCCCCCGCATCCCCC | - | 7.33 | ZNF263 | MA0528.1 | chr17:39940636-39940657 | CCTACCTTCTCCTCCTCCCCC | - | 7.62 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_23177 | chr17:39940171-39943078 | Colon_Crypt_1 | SE_23845 | chr17:39940284-39943074 | Colon_Crypt_2 | SE_24826 | chr17:39940186-39940762 | Colon_Crypt_3 | SE_24826 | chr17:39941043-39943220 | Colon_Crypt_3 | SE_26576 | chr17:39937446-39946643 | Esophagus | SE_27684 | chr17:39940016-39944181 | Fetal_Intestine | SE_28604 | chr17:39939290-39944303 | Fetal_Intestine_Large | SE_31640 | chr17:39940077-39943753 | Gastric | SE_35990 | chr17:39939244-39944308 | HMEC | SE_40900 | chr17:39937341-39943942 | Left_Ventricle | SE_41716 | chr17:39940081-39943081 | LNCaP | SE_42558 | chr17:39937451-39943776 | Lung | SE_47748 | chr17:39940258-39940577 | Pancreas | SE_47748 | chr17:39940822-39943075 | Pancreas | SE_48895 | chr17:39940059-39943716 | Right_Atrium | SE_49575 | chr17:39940710-39941117 | Right_Ventricle | SE_49575 | chr17:39941148-39943079 | Right_Ventricle | SE_50269 | chr17:39940113-39944232 | Sigmoid_Colon | SE_52578 | chr17:39940064-39943923 | Small_Intestine | SE_56909 | chr17:39940155-39943059 | VACO_400 | SE_57643 | chr17:39940618-39943012 | VACO_503 | SE_58007 | chr17:39940842-39943111 | VACO_9m | SE_64699 | chr17:39939300-39943189 | NHEK | SE_68966 | chr17:39939590-39943107 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 39941400 | 39942611 | chr17 | 39940539 | 39940600 | chr17 | 39940637 | 39940800 |
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Enhancer Sequence | GGTCACTGAG GCTCAGGTAA TGAGAGACAG AGCTGGGTCT CAAACCCAGC TCAGTTCAAG 60 CCCAAAGCCC TGTGCTCAGA ACTGCCCCAC TGTCCCATCT CTCCAAATAA ACAGTCCTTC 120 TGTAGACTAG TCAATTGACC CATCTCACTC TAAGGTGGCT CCAGGATGGG AAAAAGGTTG 180 GCAGCCCTAG CCCGACCTTT TTCGTTCCTA TGCACTGCAT TCTCAAAGCC TCGGCCCTGG 240 CAGCCCAAAC AGAGGCTCCA GAGGGAATGG GGTGGAGCCA GGGTGCAAGG GAGGGGTGGA 300 GTGGGGGTGG GAGGGCTCAA GTCACCCAAG CTGGGGCTTG ATCTAGCAAG AAATGACTAA 360 CTGGGTCCTA CCTTCTCCTC CTCCCCCGCA TCCCCCAGTC CAGTCAGTGG CCAGTTTTCA 420 CCAAGCACCT CCTAGCAGTA CTTCCTCAGT ATTATCTTTT CATCACAGCC ACAAACCAGA 480 TTAGCTAAAC TAATCATGTA GCCAACATAA TTACAATGCC CTCCCCTCCT CCACCTTGGC 540 ACAGAGAAGA GGGAAAGCAG GTTATTTTTG CCCAAACTCC CTGCTCCTGT TGCTCCCCAG 600 AGGTGCAGAA TCCCATCCCC CGGCAGAAAA GGATCTGAGT TCCCACACTG ACTTCCCCCT 660 AGCACAGGGC TGAGCGTGAT CCCCACCCAG GATAAAGGGG CTGAGTCTGG GCCCCCAGCC 720 TCACTCCCCC ATCTACAACA AAGAAAGAGG TGGTAGACTC TTCCCCTCCA AGCACTCTCG 780 ATCCCCGCCC CCCACAATCT TTCTCCCACC CCCAGGACTG AGAGAGAACC CAACTGTTGT 840 ATTCTCTCTC TGTTCCCCAA CGAGGCTGGG CTCCAAATCC TGCAAAAAGA CCACATTTCA 900 GATTTTTTTT TTAAACCGGG GTACAAACCC TGATCAAGAT CCCCAATTCT GGGTGGGGGG 960 GGGCGGTCTC AGGAAATTGG GAGCAGGGAA GGCAGGGGGC CCGATGCAGC TCTGCCTGAG 1020 AGAGTCTAGC ATTGAAGAAA CCTTCCCCCA AAAAGCCTTC CTGCGGTCTC ACTTTCCCTG 1080 TCAAATTCTT TCAGGAAAGC GGGTGGGAAA GGTCTGTGCA GGCCTCCAGA AAGCATGCAC 1140 CTTCACAATT CAGAAATCAA ATGGAAGGCA AGTCCCACAG CCTCATGCGC TTCTGCCTCA 1200 ATAACCAGCC AGCTAAGTAA TGTGGGGGAT GGGGTAGAGG CAAAAAAAAA AAGACAAGAA 1260 CAACCACTCC CCCCACCTTC CTCAGTTTGG CCCAGCCCTG CCCCACCCCC ATTCCTGGGG 1320 AGGGGGCAGA GCTTGAGAGA CAACCACTTA CGCAGGCCTT GTCTGAGGGG GTGTGGTGGT 1380 CCCAGGAGGC AGGAAGAGAA GGAAGAAGCT GCTTCCCCTC TCAGCACTTT CCACCCCCCA 1440 CCCCGGCCCC TACCTCAGGC CCCTGGGGCC CAGCGAACAG GATGAATGTG GGGGCAGGGA 1500 AGACAGGGTC GGAGCCCAGG CACCGGCCCA GGTTCAGCCA GGGGCCGGCT GGGGGAAGGG 1560 GTTTTGCACC AGGAAGGACC CCCTAAGCCT AAAGGAAGTT TTGGGCAAGG AGACGGGAAA 1620 ACCCCCAGAT AAAGCTGCTG TGAATACTTC CTCCTGCAAA GTTTGTTTTG GGTGATTTTT 1680 TCCAACAATA AGAGGTTAGA GAAGACGGGT CCTGTTCCCC TACCAACACT CTGGCAGCCA 1740 CAGCTACTGG AAACTGGGCC AGGTGACCCT GAATTCTTCA TCCGTGCACA GACCCCACCC 1800 CCCAGACCCC AGGGCGAGCC ACGGGTGCCA GACACCAGCT GGACACTGAG CCGAGCCCTG 1860 CACCCCCCAG TCACTCCATC CCACCTCCGC TGAAGAAGCC AGAGCCGGGC TCCCACCGGC 1920 GTGGAGGGAG GCGCCGCAGG TAGTATCGAC GAGGCTCTGG GAGCTGGAGG GCAGGGCCTC 1980 TGGACTCCGT GCGCTCACCT GCTCGGCAGG TGGGGCCAGA GTCGCTGGGA AAATGTGCGC 2040 TCGGCCCCCA CAGTTGGGCA AGCTGGGCGC AAACAATAGG GCCCCACCCA GGCCTGGGGG 2100 AGTAGGGAGG GAGGGAAAGC GAGGATGACG CGTGGGGTGG GGTGAGGGTG GCCCCAAAGA 2160 GACCAGCGGC AGCAAGTTCC CCAAACGGTA AATTCCTGAC TGCAGCGTGA GCCCTGGGAC 2220 GCAGTCGAAG CAGAGCAAAG TCTCCCCCGC CAGCCCAGGG CGAGAGTCAG GGACGCGGCG 2280 TCGGGCGAGC TGCGCGGGCC CCGGGGGAGG CGCGACCCCG GAGGCACCTG TCCGGATCCC 2340 TCCCCGCCTT GCTCAGATCT CTGGTTCGCG GAGCTCCGAG GCGCGCTCGG CCCGAACCGC 2400 GCGACCCCCA AGTCGCCGCG CCCAGGACCC CAGCGCGCCC CCTGCCGCCG GTGCAGGGTG 2460 GCGCTCGATG GCACCGGCCC TCACCTGCCC AGGGACGGCT GGGACCGGCC CCGCGGCCGC 2520 TCGCCACCCC TCTGTCCCCA ACGATACCTG CGCCCCCGAT 2560
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