Tag | Content |
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EnhancerAtlas ID | HS092-24487 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:102842590-102845460 |
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 | CTACGTTGTT GGCAAATTTA GGGAAAGGAA TCTCCTTGGA ACTGCCTGTG CTTTAGAGAA 60 ATGATTTGTC CCTAATCACC AGCATCATTT GGTCAGATAA GGCTTGCAGG CTCGTAGTGA 120 TTGAGGAAAT ATTTGCTAAG CTGCAGGAGG AGATCATCTT CTAAGTCCTG CTGCAACCAT 180 GTTACAAAAG TTTCCACGTC CATCCTCCGT CCACTGCGGG AAAGTTTCTC CGAAACCAAA 240 GTGCTCTCCA TCCATGATGT GTGCTCAGCA CAGTGGGTAC TTTCTCAGAA TCTGGGTCAT 300 GGAGAGGGAT GAGCTGCCTG CGGTTGGAGC TCTCTCTAGG CCCTGTACTT GGTGCCTGAA 360 GGGATTTAAG TCTTCAACTC TCAGATATGG AGAGAGATCA AACCAAGTTT GAATGTGACT 420 TCTCCACTTA CTCCCTATGT AAACTTAGAA AGATGTTTAA CTTTCTTCTA TTTCTCAGCT 480 ATAGAAAGGA ATAGAGGAAG GAAGGAAGGA GACAGGGAGG GAGGAAAGAA AGAGAGAGAG 540 AGGGAGGAAG GAAAGGAGAG AGGGAGGGAA AACGGAGGGA AGAAGGGAGT TTCGTAGAAA 600 AGAAACTAAA GAAAGCAGGG GAGAGAGATG GAGGAGAAGG GAGGAAGGGA AGAAAGAAGG 660 AAGGGAAGAA AAAAGAAAGA AACAAAGAAA GGGACAGTGA TTAAATCCTG CTTTTTGACA 720 GTGGGAATAA CTGAGTTGAA GTACAGGGAA GCATTCAGCG GGGCCTGGGC CACAGGGCGG 780 CCTCTATTGC TTGTCTGGAG GTCAAAACAA ATCCCCAACA CCACAGCTGT GGGTTTTAGT 840 CTGTGGGCCT ATGTCCTGCC AGTGCTGTTT GGCATAGAAA TGCCTCAGTG TGATCCTGAC 900 TCTCTGAGAG CCTGGCATTT CCCACCATGG TGCTTGTGAC TATGCTACTT TTGTTTTGTT 960 TTGTTTTGTT TTGTCTTAGA ACAGATACAA TCTATTAAGG CCTTGCAAAA GTAATAAATC 1020 TGCTCTAAAG TCCCCTAATT AGATGAAAAA AGAAGCCTGG TGCAGCTGAT CTGTGTGGAG 1080 ATGCACGACT TTATACCTTT TAAGTCCAGA GGCCTGAGTG ACAAGAGCAG GAAAGGGAGG 1140 GAAACTGGTT GTCTGAGAAC GTTTTATGGG CCAGCTAAAA CATAAAAGAG GTCACTGGCA 1200 TCAAGTGCTT GCTTTGCACA TAAAATACAC AGTACGGTTG TTGCCCACAT GTTTGATAAA 1260 ACGTGGCTAT TCACTAACTT GGATTTTTTC CAAATTAAAT TTCTGAATTC AGAATTAGCA 1320 ACCCTGAGCA ATGTAGAAAG CGATAAACTC CTTTTTAATG ACAAAAGTCA TCTGAACCTT 1380 AAGTGTCCAG TGCAACCTGA AGTGCTGCTA GTACTGTGGA TAGTCCGACT GGGCATGGGG 1440 AGGGGGTCTC TGGTTTTGGC TCTGGCATCT GCAGAGGCCG CCCCGTCTAA GCACACCCAT 1500 GACTGCTCTC TCCTGCTTGC GTCTTTGAGA AGAAGACAGT TCAGTCCCCC ACCACTGATT 1560 GTTTTCTGAC ACAGAGTTGA GTGGTTCAGT TGCTTTCTAC TTTTTGACTA ACAGAAGCCT 1620 GCGTCACTTT ACGTATTCTT CCTGGAAGCT CAGGCCCCAT GGTGTGTCTC TCTCACTGTC 1680 TCTCTCTCTC ACTGACTCTG TCAGTGACTC TCTCACTGAG TCATTGCGAC TCCCAGGAGC 1740 GTGACTATAG CTGTGACTTA TGGGTGTTGT GCAGTGTGTG GGGAAGCTGC TAGTGAGGTC 1800 GAGTTTAGCA GGAAGAGAAA ACAGGAATAG TGACTCACAC GGAGTAGTGG GGGCTGGGCA 1860 GATGAGAGAG TTAGGCAGCC CCGCCCTCTG CTGAGACTGG GACGCAGCCC AGATTCTGCA 1920 ACAGTGGGCA GAGGATTTGG CGATGGAGGC TAACAGGCAG CCAGGGGTCC TTTTTTTCTT 1980 TATTTTTATT TTGCTTAATT CAGAAAAGTA TGTGTGCATT TTGTGATGAA ATTCTCTACA 2040 GCTCTGTCTA CGAGAACTGC CCTGTAATAT CTCTGTGTGT TGGCTTTAAC AGTGAGCTAC 2100 TGATGAGATT CTGAGATTAG TCCCAGATCT TGTTTATGTC CTTGTTCCCC TTGAGGATAT 2160 TTTCTGAGTT AAATCAGGAA ATACCGATTA ATGGATGAAA ATGAGAAAGA GAGAAATAAT 2220 GTCCTTCGTA GGATAAGTCA TTTACCCTGA CTAGGTTAGC TAAGCTGTAT CACTCAATTA 2280 ATAATTAGGT GTGCATGACT CACCATTTTA GAAGGAGCCA TTGACAGCCC TAGCTGAAGT 2340 CAGCAAGTTC TGTATCTTCT CTAGCAAGCC ACTGGAGCTT TACAAATTCT CCTGGCAGGG 2400 GTGCATGTGT GTACGAGGAT GGAAGGGTCT GTGCACGGAT CTCCTAGAGA GATTTGAAAA 2460 TGCCTCGCCT TACTCCAGAT AGGTCTTTGG AGAATGTGCA TGTAGGATAG AATGGCTAAA 2520 ACGAAGACAA GCCAAACAGT TAGAGTGATC AAAGGGAAAC CAAGGGGACA ATGGGAAAAC 2580 AAGTCGGGGT AGAGTTAATG ACACCTTTAA CAATTATTAA AGGTGAATTT GCTTTTCAAG 2640 CTAAAGCAAA GGCAATGACA AGATCCACTG TGTGCCATTC ACAACAACCT TTCAGATTTT 2700 CATGAGAGAA CATGGCTTTT TCTGAGACTA ATTTCCAAAG GCAGATTTTT TTTCCCCCAC 2760 AGGGAGTCCT CATTTCAAAA GGGCATGGTG TAGGGAAGCT TGACTGCAAC AACTTTCCCA 2820 TGGTAAATGT CATAGCGTGT TTTGTGTGGC TTTTCTTCTA GTGTTTTCTA 2870
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