Tag | Content |
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EnhancerAtlas ID | HS051-11769 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr17:39940230-39942830 |
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 | ACTGGGTAGA TAGGTATTAG TATTCCCATT TTGCCAAAGA GGTCACTGAG GCTCAGGTAA 60 TGAGAGACAG AGCTGGGTCT CAAACCCAGC TCAGTTCAAG CCCAAAGCCC TGTGCTCAGA 120 ACTGCCCCAC TGTCCCATCT CTCCAAATAA ACAGTCCTTC TGTAGACTAG TCAATTGACC 180 CATCTCACTC TAAGGTGGCT CCAGGATGGG AAAAAGGTTG GCAGCCCTAG CCCGACCTTT 240 TTCGTTCCTA TGCACTGCAT TCTCAAAGCC TCGGCCCTGG CAGCCCAAAC AGAGGCTCCA 300 GAGGGAATGG GGTGGAGCCA GGGTGCAAGG GAGGGGTGGA GTGGGGGTGG GAGGGCTCAA 360 GTCACCCAAG CTGGGGCTTG ATCTAGCAAG AAATGACTAA CTGGGTCCTA CCTTCTCCTC 420 CTCCCCCGCA TCCCCCAGTC CAGTCAGTGG CCAGTTTTCA CCAAGCACCT CCTAGCAGTA 480 CTTCCTCAGT ATTATCTTTT CATCACAGCC ACAAACCAGA TTAGCTAAAC TAATCATGTA 540 GCCAACATAA TTACAATGCC CTCCCCTCCT CCACCTTGGC ACAGAGAAGA GGGAAAGCAG 600 GTTATTTTTG CCCAAACTCC CTGCTCCTGT TGCTCCCCAG AGGTGCAGAA TCCCATCCCC 660 CGGCAGAAAA GGATCTGAGT TCCCACACTG ACTTCCCCCT AGCACAGGGC TGAGCGTGAT 720 CCCCACCCAG GATAAAGGGG CTGAGTCTGG GCCCCCAGCC TCACTCCCCC ATCTACAACA 780 AAGAAAGAGG TGGTAGACTC TTCCCCTCCA AGCACTCTCG ATCCCCGCCC CCCACAATCT 840 TTCTCCCACC CCCAGGACTG AGAGAGAACC CAACTGTTGT ATTCTCTCTC TGTTCCCCAA 900 CGAGGCTGGG CTCCAAATCC TGCAAAAAGA CCACATTTCA GATTTTTTTT TTAAACCGGG 960 GTACAAACCC TGATCAAGAT CCCCAATTCT GGGTGGGGGG GGGCGGTCTC AGGAAATTGG 1020 GAGCAGGGAA GGCAGGGGGC CCGATGCAGC TCTGCCTGAG AGAGTCTAGC ATTGAAGAAA 1080 CCTTCCCCCA AAAAGCCTTC CTGCGGTCTC ACTTTCCCTG TCAAATTCTT TCAGGAAAGC 1140 GGGTGGGAAA GGTCTGTGCA GGCCTCCAGA AAGCATGCAC CTTCACAATT CAGAAATCAA 1200 ATGGAAGGCA AGTCCCACAG CCTCATGCGC TTCTGCCTCA ATAACCAGCC AGCTAAGTAA 1260 TGTGGGGGAT GGGGTAGAGG CAAAAAAAAA AAGACAAGAA CAACCACTCC CCCCACCTTC 1320 CTCAGTTTGG CCCAGCCCTG CCCCACCCCC ATTCCTGGGG AGGGGGCAGA GCTTGAGAGA 1380 CAACCACTTA CGCAGGCCTT GTCTGAGGGG GTGTGGTGGT CCCAGGAGGC AGGAAGAGAA 1440 GGAAGAAGCT GCTTCCCCTC TCAGCACTTT CCACCCCCCA CCCCGGCCCC TACCTCAGGC 1500 CCCTGGGGCC CAGCGAACAG GATGAATGTG GGGGCAGGGA AGACAGGGTC GGAGCCCAGG 1560 CACCGGCCCA GGTTCAGCCA GGGGCCGGCT GGGGGAAGGG GTTTTGCACC AGGAAGGACC 1620 CCCTAAGCCT AAAGGAAGTT TTGGGCAAGG AGACGGGAAA ACCCCCAGAT AAAGCTGCTG 1680 TGAATACTTC CTCCTGCAAA GTTTGTTTTG GGTGATTTTT TCCAACAATA AGAGGTTAGA 1740 GAAGACGGGT CCTGTTCCCC TACCAACACT CTGGCAGCCA CAGCTACTGG AAACTGGGCC 1800 AGGTGACCCT GAATTCTTCA TCCGTGCACA GACCCCACCC CCCAGACCCC AGGGCGAGCC 1860 ACGGGTGCCA GACACCAGCT GGACACTGAG CCGAGCCCTG CACCCCCCAG TCACTCCATC 1920 CCACCTCCGC TGAAGAAGCC AGAGCCGGGC TCCCACCGGC GTGGAGGGAG GCGCCGCAGG 1980 TAGTATCGAC GAGGCTCTGG GAGCTGGAGG GCAGGGCCTC TGGACTCCGT GCGCTCACCT 2040 GCTCGGCAGG TGGGGCCAGA GTCGCTGGGA AAATGTGCGC TCGGCCCCCA CAGTTGGGCA 2100 AGCTGGGCGC AAACAATAGG GCCCCACCCA GGCCTGGGGG AGTAGGGAGG GAGGGAAAGC 2160 GAGGATGACG CGTGGGGTGG GGTGAGGGTG GCCCCAAAGA GACCAGCGGC AGCAAGTTCC 2220 CCAAACGGTA AATTCCTGAC TGCAGCGTGA GCCCTGGGAC GCAGTCGAAG CAGAGCAAAG 2280 TCTCCCCCGC CAGCCCAGGG CGAGAGTCAG GGACGCGGCG TCGGGCGAGC TGCGCGGGCC 2340 CCGGGGGAGG CGCGACCCCG GAGGCACCTG TCCGGATCCC TCCCCGCCTT GCTCAGATCT 2400 CTGGTTCGCG GAGCTCCGAG GCGCGCTCGG CCCGAACCGC GCGACCCCCA AGTCGCCGCG 2460 CCCAGGACCC CAGCGCGCCC CCTGCCGCCG GTGCAGGGTG GCGCTCGATG GCACCGGCCC 2520 TCACCTGCCC AGGGACGGCT GGGACCGGCC CCGCGGCCGC TCGCCACCCC TCTGTCCCCA 2580 ACGATACCTG CGCCCCCGAT 2600
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