Tag | Content |
---|
EnhancerAtlas ID | HS091-02434 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr1:109431220-109433520 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:109431977-109431995 | GGAACAAAGGAAGGAGGA | + | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I108889 | chr1 | 109431823 | 109432622 |
| Enhancer Sequence | TCAAGTGCTG GGATTACAGG AATGAGCTGC CGTGCCCAGC TGGTAATAGA TTCTTTATCA 60 AAACTGTTAC AAGTTAATTA TTAGATGAAC ATCAGAATAT AGTAGCAATT AATAGAATTC 120 AAAATCTCAG GAGGGTGTAC CAAATTTTAG ATGTCTTAAC ATATTTAGGA AATGGGAGAT 180 TTATCATCCT GTAAATAGTT CACGTTAGGA AGGTTCATGC CAAGGAAGTT AACATAGGTA 240 AGATGAGGAC ATTTCTATTA AAAAAGAGTT TCAAGTAAAA TAAAATGGAA GACATTTAAG 300 ATAATTAAGA TGAGCTTTTA ATATACGAAA TGCTGCCATC CTACCCTTTA CATAAATTTC 360 CAGAAACCTG GGAATTATAT ACTTTTTTCT TTTCTCATTC TGTATCCAGC ATGAAGTATT 420 GCTGGTTTCA TCTCCTAAAT GTTTCTCAGA TTCATCTACT CATGTGCATC CTCCCAGTTG 480 TTTGAAAGGC TTGTTCCCCG GTGCTGTAAA GAAATAGCAC TTGAACATAA ATTTAATTTA 540 TTTAGTAAGG CCATTTTTAC TTGCTGCAGA AGGGGTACAC TCATCAGCAG TTTTGCCTCG 600 AGAGTACACT GAACAAAGGA GACAGGGTCA TTTATAACCT GATGTATCCA CCCTACTGCT 660 GTGTCTGGTT TCCATTAACT GGAACGGGAC CTCACATTCT GTATTTGTCC CGATTGGCTA 720 GCAACTTAGA ACTTTTTAAA AGAGGCAAAG GTAGAGGGGA ACAAAGGAAG GAGGAAGTAA 780 CTTGTGGAAT GTTGAGAAAG ATAAAAACAC TTTTAAATAA GGAAGAGGAA CAGGCTATGA 840 CCTAATGCTT GCTTGGACCA GTGTAAGCAT GCTAGGGCAA ATACTTAGGC TAAATTGTGG 900 GAGCTAAGAA CATAAGGTAC ATTGATTTCC TTATTACCGC TAGCAGATAT TTAAGAATGT 960 TAACACAGTT CTTTGAATAA ATTTTGCGTC TAAGGAATAA ATACTATTTA TTCCTAATTA 1020 GATGGGGAGG AAAGTCTTTG AAGAGGAACC TTTACTTTAC TTTTTACACC GCCATAGCTA 1080 TAATTGAGAT CCTCAGGATC TTCTTTCCAG ACTGCCTCCA TTCTTCACCT CTTGGAACCC 1140 GTCGTTTTGA CTTGTCACTA GTGGGCTCAA TCTCAAAACA CAGAGCTAAC CGTGCAACCT 1200 CTCTGCTTAA TACCTAGGGT GGCTCCTAGT CACCCGGCCA AGCTGAACAT AGAACACAAG 1260 ATCTTCATTA TCTGGCTTCT GCCTATTCCT GGGACCTTAC TTCCTGCCAT TCTTCACCTT 1320 GCACTTTGAG CTCTGGTTTC CTGCATGTCA TGCTGTTTTA TATTTCAGTG TCTTTGCTCA 1380 TGCTATGCCC TATGTTGAAC TCCCTTCCCA CTTTCTTTGT TTAGCTAATT CTACTCTAAG 1440 ATACAGCTCG GAGATTATCT CCTCCTGGAA ACCATTTCTA AGCTCCATAG TTAGGCTCTG 1500 TGGCCTCCGT GTGCTCATAT TACAATCTGT GCATTTTTCT TTCTTAGCAC CAACTGTATT 1560 AAAATTAAGT TAATCTGTTT TTATGGTGCT CCCTTCCTCC TCACCTCTCC CTTTGAGCAT 1620 TAGCTCCTCA GCTGTGGTCA CTCCTCAGCA GCCATGATAA TTAGCATGTT GTCTGGCACA 1680 TATTGAACTT CAATGGAATA TGAACGTAAT AAGATGTTTA TCTGTCTTGC TAAATGTTTT 1740 GAATAGTATT GTGCTTTCTA ATATGGTAAG AACAGTAGAT AAGTAGGAAT GGCTTGTACC 1800 TCTGCCTGTT GGAAGATCTT AGAATTGTCC TTTTTCTGTG ATACAGTCTA GATCAAACAT 1860 GGTTGCACTT TGCTATAGGA CTTCACCAAG GGAAACTTAA AAATCTGTAC TGTCTGTAAT 1920 AGGACTATAC CAAACAAATC TCTGGCTTTA TCAGTGCTCT AAGACCAGCA TTCTGTATAT 1980 TGATTGGATT GTCGTATAAT TGGGGGTAAT GATTTGAACT CTTTATGTTA GGCCATAGGC 2040 TGGTATAAGT TATTCTTCTG CTATAGTAAA TCCTTATGAA ATGTTTTATC CATCTGGTTC 2100 TTCCATTGTG GAGGTCCTCC TCTATCCCTG GAGGAGTTTC TGTGGCACAA TGAATTTGTA 2160 ATTTTGAATG GAATGTTTCT TGGAACACTA AGTAACCTCC TAAGGGGACA TCAGAATGCT 2220 TTATTGAAAT ATTTTGCACC TATTTCAAAA GGTAGAGACT GATAGCAAGT ACAATTTAAG 2280 TTAAAAAAAA ATTATATGGT 2300
|
| |
|
|
|