Tag | Content |
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EnhancerAtlas ID | HS154-12694 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr2:102842740-102845620 |
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 | chr2:102843224-102843242 | AGAAGGGAGGAAGGGAAG | + | 6.05 | EWSR1-FLI1 | MA0149.1 | chr2:102843104-102843122 | GGGAGGGAGGAAAGAAAG | + | 6.23 | EWSR1-FLI1 | MA0149.1 | chr2:102843228-102843246 | GGGAGGAAGGGAAGAAAG | + | 6.25 | EWSR1-FLI1 | MA0149.1 | chr2:102843127-102843145 | GAGAGGGAGGAAGGAAAG | + | 6.42 | EWSR1-FLI1 | MA0149.1 | chr2:102843232-102843250 | GGAAGGGAAGAAAGAAGG | + | 6.62 | EWSR1-FLI1 | MA0149.1 | chr2:102843236-102843254 | GGGAAGAAAGAAGGAAGG | + | 6.72 | EWSR1-FLI1 | MA0149.1 | chr2:102843081-102843099 | TAGAGGAAGGAAGGAAGG | + | 6.84 | EWSR1-FLI1 | MA0149.1 | chr2:102843077-102843095 | GGAATAGAGGAAGGAAGG | + | 7.01 | EWSR1-FLI1 | MA0149.1 | chr2:102843085-102843103 | GGAAGGAAGGAAGGAGAC | + | 7.67 | ZNF263 | MA0528.1 | chr2:102843245-102843266 | GAAGGAAGGGAAGAAAAAAGA | + | 6.06 | ZNF263 | MA0528.1 | chr2:102843141-102843162 | AAAGGAGAGAGGGAGGGAAAA | + | 6.09 | ZNF263 | MA0528.1 | chr2:102843090-102843111 | GAAGGAAGGAGACAGGGAGGG | + | 6.17 | ZNF263 | MA0528.1 | chr2:102843216-102843237 | GATGGAGGAGAAGGGAGGAAG | + | 6.25 | ZNF263 | MA0528.1 | chr2:102843106-102843127 | GAGGGAGGAAAGAAAGAGAGA | + | 6.3 | ZNF263 | MA0528.1 | chr2:102843226-102843247 | AAGGGAGGAAGGGAAGAAAGA | + | 6.64 | ZNF263 | MA0528.1 | chr2:102843713-102843734 | AGAGCAGGAAAGGGAGGGAAA | + | 6.65 | ZNF263 | MA0528.1 | chr2:102843094-102843115 | GAAGGAGACAGGGAGGGAGGA | + | 6.7 | ZNF263 | MA0528.1 | chr2:102843132-102843153 | GGAGGAAGGAAAGGAGAGAGG | + | 6.94 | ZNF263 | MA0528.1 | chr2:102843229-102843250 | GGAGGAAGGGAAGAAAGAAGG | + | 7.06 | ZNF263 | MA0528.1 | chr2:102843219-102843240 | GGAGGAGAAGGGAGGAAGGGA | + | 7.12 | ZNF263 | MA0528.1 | chr2:102843222-102843243 | GGAGAAGGGAGGAAGGGAAGA | + | 7.12 | ZNF263 | MA0528.1 | chr2:102843129-102843150 | GAGGGAGGAAGGAAAGGAGAG | + | 7.51 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 102843334 | 102845009 | chr2 | 102844840 | 102845062 | chr2 | 102844003 | 102844653 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I102226 | chr2 | 102842670 | 102846324 |
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Enhancer Sequence | AGATCATCTT CTAAGTCCTG CTGCAACCAT GTTACAAAAG TTTCCACGTC CATCCTCCGT 60 CCACTGCGGG AAAGTTTCTC CGAAACCAAA GTGCTCTCCA TCCATGATGT GTGCTCAGCA 120 CAGTGGGTAC TTTCTCAGAA TCTGGGTCAT GGAGAGGGAT GAGCTGCCTG CGGTTGGAGC 180 TCTCTCTAGG CCCTGTACTT GGTGCCTGAA GGGATTTAAG TCTTCAACTC TCAGATATGG 240 AGAGAGATCA AACCAAGTTT GAATGTGACT TCTCCACTTA CTCCCTATGT AAACTTAGAA 300 AGATGTTTAA CTTTCTTCTA TTTCTCAGCT ATAGAAAGGA ATAGAGGAAG GAAGGAAGGA 360 GACAGGGAGG GAGGAAAGAA AGAGAGAGAG AGGGAGGAAG GAAAGGAGAG AGGGAGGGAA 420 AACGGAGGGA AGAAGGGAGT TTCGTAGAAA AGAAACTAAA GAAAGCAGGG GAGAGAGATG 480 GAGGAGAAGG GAGGAAGGGA AGAAAGAAGG AAGGGAAGAA AAAAGAAAGA AACAAAGAAA 540 GGGACAGTGA TTAAATCCTG CTTTTTGACA GTGGGAATAA CTGAGTTGAA GTACAGGGAA 600 GCATTCAGCG GGGCCTGGGC CACAGGGCGG CCTCTATTGC TTGTCTGGAG GTCAAAACAA 660 ATCCCCAACA CCACAGCTGT GGGTTTTAGT CTGTGGGCCT ATGTCCTGCC AGTGCTGTTT 720 GGCATAGAAA TGCCTCAGTG TGATCCTGAC TCTCTGAGAG CCTGGCATTT CCCACCATGG 780 TGCTTGTGAC TATGCTACTT TTGTTTTGTT TTGTTTTGTT TTGTCTTAGA ACAGATACAA 840 TCTATTAAGG CCTTGCAAAA GTAATAAATC TGCTCTAAAG TCCCCTAATT AGATGAAAAA 900 AGAAGCCTGG TGCAGCTGAT CTGTGTGGAG ATGCACGACT TTATACCTTT TAAGTCCAGA 960 GGCCTGAGTG ACAAGAGCAG GAAAGGGAGG GAAACTGGTT GTCTGAGAAC GTTTTATGGG 1020 CCAGCTAAAA CATAAAAGAG GTCACTGGCA TCAAGTGCTT GCTTTGCACA TAAAATACAC 1080 AGTACGGTTG TTGCCCACAT GTTTGATAAA ACGTGGCTAT TCACTAACTT GGATTTTTTC 1140 CAAATTAAAT TTCTGAATTC AGAATTAGCA ACCCTGAGCA ATGTAGAAAG CGATAAACTC 1200 CTTTTTAATG ACAAAAGTCA TCTGAACCTT AAGTGTCCAG TGCAACCTGA AGTGCTGCTA 1260 GTACTGTGGA TAGTCCGACT GGGCATGGGG AGGGGGTCTC TGGTTTTGGC TCTGGCATCT 1320 GCAGAGGCCG CCCCGTCTAA GCACACCCAT GACTGCTCTC TCCTGCTTGC GTCTTTGAGA 1380 AGAAGACAGT TCAGTCCCCC ACCACTGATT GTTTTCTGAC ACAGAGTTGA GTGGTTCAGT 1440 TGCTTTCTAC TTTTTGACTA ACAGAAGCCT GCGTCACTTT ACGTATTCTT CCTGGAAGCT 1500 CAGGCCCCAT GGTGTGTCTC TCTCACTGTC TCTCTCTCTC ACTGACTCTG TCAGTGACTC 1560 TCTCACTGAG TCATTGCGAC TCCCAGGAGC GTGACTATAG CTGTGACTTA TGGGTGTTGT 1620 GCAGTGTGTG GGGAAGCTGC TAGTGAGGTC GAGTTTAGCA GGAAGAGAAA ACAGGAATAG 1680 TGACTCACAC GGAGTAGTGG GGGCTGGGCA GATGAGAGAG TTAGGCAGCC CCGCCCTCTG 1740 CTGAGACTGG GACGCAGCCC AGATTCTGCA ACAGTGGGCA GAGGATTTGG CGATGGAGGC 1800 TAACAGGCAG CCAGGGGTCC TTTTTTTCTT TATTTTTATT TTGCTTAATT CAGAAAAGTA 1860 TGTGTGCATT TTGTGATGAA ATTCTCTACA GCTCTGTCTA CGAGAACTGC CCTGTAATAT 1920 CTCTGTGTGT TGGCTTTAAC AGTGAGCTAC TGATGAGATT CTGAGATTAG TCCCAGATCT 1980 TGTTTATGTC CTTGTTCCCC TTGAGGATAT TTTCTGAGTT AAATCAGGAA ATACCGATTA 2040 ATGGATGAAA ATGAGAAAGA GAGAAATAAT GTCCTTCGTA GGATAAGTCA TTTACCCTGA 2100 CTAGGTTAGC TAAGCTGTAT CACTCAATTA ATAATTAGGT GTGCATGACT CACCATTTTA 2160 GAAGGAGCCA TTGACAGCCC TAGCTGAAGT CAGCAAGTTC TGTATCTTCT CTAGCAAGCC 2220 ACTGGAGCTT TACAAATTCT CCTGGCAGGG GTGCATGTGT GTACGAGGAT GGAAGGGTCT 2280 GTGCACGGAT CTCCTAGAGA GATTTGAAAA TGCCTCGCCT TACTCCAGAT AGGTCTTTGG 2340 AGAATGTGCA TGTAGGATAG AATGGCTAAA ACGAAGACAA GCCAAACAGT TAGAGTGATC 2400 AAAGGGAAAC CAAGGGGACA ATGGGAAAAC AAGTCGGGGT AGAGTTAATG ACACCTTTAA 2460 CAATTATTAA AGGTGAATTT GCTTTTCAAG CTAAAGCAAA GGCAATGACA AGATCCACTG 2520 TGTGCCATTC ACAACAACCT TTCAGATTTT CATGAGAGAA CATGGCTTTT TCTGAGACTA 2580 ATTTCCAAAG GCAGATTTTT TTTCCCCCAC AGGGAGTCCT CATTTCAAAA GGGCATGGTG 2640 TAGGGAAGCT TGACTGCAAC AACTTTCCCA TGGTAAATGT CATAGCGTGT TTTGTGTGGC 2700 TTTTCTTCTA GTGTTTTCTA TGCATATTGG GGGTAAACCC ACCAAACCTC CTGCAGTTCA 2760 GTAAAAGCAT TTGCGTGGAG GCCAGATTGA ATCTGAATTT TCCACTGTTC TGGTTTCATC 2820 AGGCCTAAAA TTTAGCAATA TCATATTGAG AGAAAGTAGG GAATTGAATA ATCTTTAGAC 2880
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