Tag | Content |
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EnhancerAtlas ID | HS054-00538 |
Organism | Homo sapiens |
Tissue/cell | FT246 |
Coordinate | chr1:168993780-168995080 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:168993868-168993886 | GGAAGGAAGGAGAGAGAG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr1:168993923-168993941 | GGAGGGAGGGGAGGAAGA | + | 6.41 | EWSR1-FLI1 | MA0149.1 | chr1:168993781-168993799 | GAAAGGAAGGAAGGAGAA | + | 6.46 | EWSR1-FLI1 | MA0149.1 | chr1:168993838-168993856 | GAAAGGAAGGAAGGAGAA | + | 6.46 | EWSR1-FLI1 | MA0149.1 | chr1:168993884-168993902 | AGAGGGAAGGAAGGAACG | + | 6.61 | EWSR1-FLI1 | MA0149.1 | chr1:168993829-168993847 | GGAAGGAAGGAAAGGAAG | + | 6.98 | EWSR1-FLI1 | MA0149.1 | chr1:168993825-168993843 | AGGAGGAAGGAAGGAAAG | + | 7.22 | EWSR1-FLI1 | MA0149.1 | chr1:168993904-168993922 | GGAAGGAAGGAAGGGGGA | + | 7.23 | EWSR1-FLI1 | MA0149.1 | chr1:168993834-168993852 | GAAGGAAAGGAAGGAAGG | + | 7.26 | EWSR1-FLI1 | MA0149.1 | chr1:168993860-168993878 | AGGAGGAAGGAAGGAAGG | + | 7.85 | EWSR1-FLI1 | MA0149.1 | chr1:168993864-168993882 | GGAAGGAAGGAAGGAGAG | + | 8.99 | EWSR1-FLI1 | MA0149.1 | chr1:168993888-168993906 | GGAAGGAAGGAACGAAGG | + | 9.09 | EWSR1-FLI1 | MA0149.1 | chr1:168993900-168993918 | CGAAGGAAGGAAGGAAGG | + | 9.09 | EWSR1-FLI1 | MA0149.1 | chr1:168993892-168993910 | GGAAGGAACGAAGGAAGG | + | 9.17 | EWSR1-FLI1 | MA0149.1 | chr1:168993896-168993914 | GGAACGAAGGAAGGAAGG | + | 9.17 | ZNF263 | MA0528.1 | chr1:168993865-168993886 | GAAGGAAGGAAGGAGAGAGAG | + | 6.04 | ZNF263 | MA0528.1 | chr1:168993790-168993811 | GAAGGAGAAGAGGAGGAGGAA | + | 6.11 | ZNF263 | MA0528.1 | chr1:168993812-168993833 | GAAGGAGAAGAGGAGGAGGAA | + | 6.11 | ZNF263 | MA0528.1 | chr1:168993847-168993868 | GAAGGAGAAGAGGAGGAGGAA | + | 6.11 | ZNF263 | MA0528.1 | chr1:168993795-168993816 | AGAAGAGGAGGAGGAAGGAAG | + | 6.1 | ZNF263 | MA0528.1 | chr1:168993817-168993838 | AGAAGAGGAGGAGGAAGGAAG | + | 6.1 | ZNF263 | MA0528.1 | chr1:168993852-168993873 | AGAAGAGGAGGAGGAAGGAAG | + | 6.1 | ZNF263 | MA0528.1 | chr1:168993830-168993851 | GAAGGAAGGAAAGGAAGGAAG | + | 6.23 | ZNF263 | MA0528.1 | chr1:168993826-168993847 | GGAGGAAGGAAGGAAAGGAAG | + | 6.27 | ZNF263 | MA0528.1 | chr1:168993827-168993848 | GAGGAAGGAAGGAAAGGAAGG | + | 6.34 | ZNF263 | MA0528.1 | chr1:168993924-168993945 | GAGGGAGGGGAGGAAGAGGAG | + | 6.39 | ZNF263 | MA0528.1 | chr1:168993805-168993826 | GAGGAAGGAAGGAGAAGAGGA | + | 6.63 | ZNF263 | MA0528.1 | chr1:168993905-168993926 | GAAGGAAGGAAGGGGGAGGGA | + | 6.6 | ZNF263 | MA0528.1 | chr1:168993798-168993819 | AGAGGAGGAGGAAGGAAGGAG | + | 6.78 | ZNF263 | MA0528.1 | chr1:168993820-168993841 | AGAGGAGGAGGAAGGAAGGAA | + | 6.87 | ZNF263 | MA0528.1 | chr1:168993855-168993876 | AGAGGAGGAGGAAGGAAGGAA | + | 6.87 | ZNF263 | MA0528.1 | chr1:168993909-168993930 | GAAGGAAGGGGGAGGGAGGGA | + | 6.97 | ZNF263 | MA0528.1 | chr1:168993869-168993890 | GAAGGAAGGAGAGAGAGAGGG | + | 7.05 | ZNF263 | MA0528.1 | chr1:168993901-168993922 | GAAGGAAGGAAGGAAGGGGGA | + | 7.14 | ZNF263 | MA0528.1 | chr1:168993861-168993882 | GGAGGAAGGAAGGAAGGAGAG | + | 7.22 | ZNF263 | MA0528.1 | chr1:168993801-168993822 | GGAGGAGGAAGGAAGGAGAAG | + | 7.24 | ZNF263 | MA0528.1 | chr1:168993873-168993894 | GAAGGAGAGAGAGAGGGAAGG | + | 7.25 | ZNF263 | MA0528.1 | chr1:168993916-168993937 | GGGGGAGGGAGGGAGGGGAGG | + | 7.95 | ZNF263 | MA0528.1 | chr1:168993823-168993844 | GGAGGAGGAAGGAAGGAAAGG | + | 7.99 | ZNF263 | MA0528.1 | chr1:168993786-168993807 | GAAGGAAGGAGAAGAGGAGGA | + | 8.04 | ZNF263 | MA0528.1 | chr1:168993808-168993829 | GAAGGAAGGAGAAGAGGAGGA | + | 8.04 | ZNF263 | MA0528.1 | chr1:168993843-168993864 | GAAGGAAGGAGAAGAGGAGGA | + | 8.04 | ZNF263 | MA0528.1 | chr1:168993935-168993956 | GGAAGAGGAGGAGGAGGAAGG | + | 8.17 | ZNF263 | MA0528.1 | chr1:168993858-168993879 | GGAGGAGGAAGGAAGGAAGGA | + | 8.47 | ZNF263 | MA0528.1 | chr1:168993920-168993941 | GAGGGAGGGAGGGGAGGAAGA | + | 8.61 | ZNF263 | MA0528.1 | chr1:168993929-168993950 | AGGGGAGGAAGAGGAGGAGGA | + | 8.78 | ZNF263 | MA0528.1 | chr1:168993932-168993953 | GGAGGAAGAGGAGGAGGAGGA | + | 9.83 |
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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 |
GH01I169024 | chr1 | 168994135 | 168994681 |
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Enhancer Sequence | GGAAAGGAAG GAAGGAGAAG AGGAGGAGGA AGGAAGGAGA AGAGGAGGAG GAAGGAAGGA 60 AAGGAAGGAA GGAGAAGAGG AGGAGGAAGG AAGGAAGGAG AGAGAGAGGG AAGGAAGGAA 120 CGAAGGAAGG AAGGAAGGGG GAGGGAGGGA GGGGAGGAAG AGGAGGAGGA GGAAGGATCT 180 CTCACATCTA CCTTCAAAAA TGTCTTCTAT TTGGAGGCAC TGGAAATAAC AAGAATAACT 240 GTAGAAAAAA CATTCATATG TTCCTGTGAG ATGCAAACTA TATTCAATGT TCCAGTCCCT 300 ATTGCTGTCA TACAAACTAC TCAACACTTA AGACAAAAAC AAACCAATTT TTTTTTTTTA 360 CTATACCCAC ATAATATGTG GGTCAGGAAT TCAGAAAAGG ACAGCTTATC TTTGTGGTAC 420 AATCTGAGCT GTCAGCTGGG AAGACTTGAA GCCTGGGGGT GACTTGACAA CAGGAGATTG 480 GAATCTTCCG AAGACTCACT CACATGTCTG GTGGTCAATA CTGACTGTTG GCTGGGTCTT 540 CAGCTGGGGC AATCAACTGG AACACCAGTT ATAGCTGAGT GGTTTTCTCA ACCAGCTCCC 600 TGTCTATAGT AATAAAGGGG GAGTCCAAAG GTCTCAGACT TTCATTTGTA CTGTTTCTGT 660 TCCTTTCTGT GCAAGTTAAT ATGATTCTTT TAAAAACTTT GTGAACTATT GGCATATTAA 720 CTTATAATTT ATCCCATTAG ACAAACAGCC ACAGCTGCAA ATCTCTCTGA GCTAAGTCTT 780 TCTCCACCTT GGGCTCCCTG TAAGGCTGTT ATGGAACAGT GACCTTAAGA TTCCTATAAG 840 TCCTATTTTT AAATAGAGAG GGAGGCAAGC TCCCAATTGC CTCTCTGTAG TGAAAACAGA 900 GTGAATCCTG GAGGAACAAT GAGGCAGGGA AGCTGAACCT GGCATTTTCA TTCAAAGTCA 960 AAAGCTACAA GGAGGGTTGC AAGTGGTGCC TCTACTGGCA GAAGTCAAAG TCAAGCCCTC 1020 TCTGGAGGAA GGGTCACCAA GTCAGACCCA TAGGACTCAC ATCTCTTTAA GCTCAAGTGA 1080 TGAACCAGTG AAGATGACCA AGCACACAAG AAGTCAAACC ACTAGTGACA ACAGATTTAG 1140 ACACCCAAGA ATTGCAAATT ACGGAATTGT CAGATTTTAA AAAAATAATT GTTATGAATG 1200 AAATCTTAAA TGAAATAAAA TATTTGCTGC AATAGCAAAA ATGAGCATAC AAGAAACCAC 1260 CAGCAGTGAA CAATCTTAAA ATACTACTCC AACTCCTGAC 1300
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