Tag | Content |
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EnhancerAtlas ID | HS187-13722 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:102842550-102845600 |
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: 4 | Chromosome | Start | End |
chr2 | 102843334 | 102845009 | chr2 | 102842650 | 102845550 | 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 | TACATATACA ACGATTTCAA ATATACTTTG TCATATTTTA CTACGTTGTT GGCAAATTTA 60 GGGAAAGGAA TCTCCTTGGA ACTGCCTGTG CTTTAGAGAA ATGATTTGTC CCTAATCACC 120 AGCATCATTT GGTCAGATAA GGCTTGCAGG CTCGTAGTGA TTGAGGAAAT ATTTGCTAAG 180 CTGCAGGAGG AGATCATCTT CTAAGTCCTG CTGCAACCAT GTTACAAAAG TTTCCACGTC 240 CATCCTCCGT CCACTGCGGG AAAGTTTCTC CGAAACCAAA GTGCTCTCCA TCCATGATGT 300 GTGCTCAGCA CAGTGGGTAC TTTCTCAGAA TCTGGGTCAT GGAGAGGGAT GAGCTGCCTG 360 CGGTTGGAGC TCTCTCTAGG CCCTGTACTT GGTGCCTGAA GGGATTTAAG TCTTCAACTC 420 TCAGATATGG AGAGAGATCA AACCAAGTTT GAATGTGACT TCTCCACTTA CTCCCTATGT 480 AAACTTAGAA AGATGTTTAA CTTTCTTCTA TTTCTCAGCT ATAGAAAGGA ATAGAGGAAG 540 GAAGGAAGGA GACAGGGAGG GAGGAAAGAA AGAGAGAGAG AGGGAGGAAG GAAAGGAGAG 600 AGGGAGGGAA AACGGAGGGA AGAAGGGAGT TTCGTAGAAA AGAAACTAAA GAAAGCAGGG 660 GAGAGAGATG GAGGAGAAGG GAGGAAGGGA AGAAAGAAGG AAGGGAAGAA AAAAGAAAGA 720 AACAAAGAAA GGGACAGTGA TTAAATCCTG CTTTTTGACA GTGGGAATAA CTGAGTTGAA 780 GTACAGGGAA GCATTCAGCG GGGCCTGGGC CACAGGGCGG CCTCTATTGC TTGTCTGGAG 840 GTCAAAACAA ATCCCCAACA CCACAGCTGT GGGTTTTAGT CTGTGGGCCT ATGTCCTGCC 900 AGTGCTGTTT GGCATAGAAA TGCCTCAGTG TGATCCTGAC TCTCTGAGAG CCTGGCATTT 960 CCCACCATGG TGCTTGTGAC TATGCTACTT TTGTTTTGTT TTGTTTTGTT TTGTCTTAGA 1020 ACAGATACAA TCTATTAAGG CCTTGCAAAA GTAATAAATC TGCTCTAAAG TCCCCTAATT 1080 AGATGAAAAA AGAAGCCTGG TGCAGCTGAT CTGTGTGGAG ATGCACGACT TTATACCTTT 1140 TAAGTCCAGA GGCCTGAGTG ACAAGAGCAG GAAAGGGAGG GAAACTGGTT GTCTGAGAAC 1200 GTTTTATGGG CCAGCTAAAA CATAAAAGAG GTCACTGGCA TCAAGTGCTT GCTTTGCACA 1260 TAAAATACAC AGTACGGTTG TTGCCCACAT GTTTGATAAA ACGTGGCTAT TCACTAACTT 1320 GGATTTTTTC CAAATTAAAT TTCTGAATTC AGAATTAGCA ACCCTGAGCA ATGTAGAAAG 1380 CGATAAACTC CTTTTTAATG ACAAAAGTCA TCTGAACCTT AAGTGTCCAG TGCAACCTGA 1440 AGTGCTGCTA GTACTGTGGA TAGTCCGACT GGGCATGGGG AGGGGGTCTC TGGTTTTGGC 1500 TCTGGCATCT GCAGAGGCCG CCCCGTCTAA GCACACCCAT GACTGCTCTC TCCTGCTTGC 1560 GTCTTTGAGA AGAAGACAGT TCAGTCCCCC ACCACTGATT GTTTTCTGAC ACAGAGTTGA 1620 GTGGTTCAGT TGCTTTCTAC TTTTTGACTA ACAGAAGCCT GCGTCACTTT ACGTATTCTT 1680 CCTGGAAGCT CAGGCCCCAT GGTGTGTCTC TCTCACTGTC TCTCTCTCTC ACTGACTCTG 1740 TCAGTGACTC TCTCACTGAG TCATTGCGAC TCCCAGGAGC GTGACTATAG CTGTGACTTA 1800 TGGGTGTTGT GCAGTGTGTG GGGAAGCTGC TAGTGAGGTC GAGTTTAGCA GGAAGAGAAA 1860 ACAGGAATAG TGACTCACAC GGAGTAGTGG GGGCTGGGCA GATGAGAGAG TTAGGCAGCC 1920 CCGCCCTCTG CTGAGACTGG GACGCAGCCC AGATTCTGCA ACAGTGGGCA GAGGATTTGG 1980 CGATGGAGGC TAACAGGCAG CCAGGGGTCC TTTTTTTCTT TATTTTTATT TTGCTTAATT 2040 CAGAAAAGTA TGTGTGCATT TTGTGATGAA ATTCTCTACA GCTCTGTCTA CGAGAACTGC 2100 CCTGTAATAT CTCTGTGTGT TGGCTTTAAC AGTGAGCTAC TGATGAGATT CTGAGATTAG 2160 TCCCAGATCT TGTTTATGTC CTTGTTCCCC TTGAGGATAT TTTCTGAGTT AAATCAGGAA 2220 ATACCGATTA ATGGATGAAA ATGAGAAAGA GAGAAATAAT GTCCTTCGTA GGATAAGTCA 2280 TTTACCCTGA CTAGGTTAGC TAAGCTGTAT CACTCAATTA ATAATTAGGT GTGCATGACT 2340 CACCATTTTA GAAGGAGCCA TTGACAGCCC TAGCTGAAGT CAGCAAGTTC TGTATCTTCT 2400 CTAGCAAGCC ACTGGAGCTT TACAAATTCT CCTGGCAGGG GTGCATGTGT GTACGAGGAT 2460 GGAAGGGTCT GTGCACGGAT CTCCTAGAGA GATTTGAAAA TGCCTCGCCT TACTCCAGAT 2520 AGGTCTTTGG AGAATGTGCA TGTAGGATAG AATGGCTAAA ACGAAGACAA GCCAAACAGT 2580 TAGAGTGATC AAAGGGAAAC CAAGGGGACA ATGGGAAAAC AAGTCGGGGT AGAGTTAATG 2640 ACACCTTTAA CAATTATTAA AGGTGAATTT GCTTTTCAAG CTAAAGCAAA GGCAATGACA 2700 AGATCCACTG TGTGCCATTC ACAACAACCT TTCAGATTTT CATGAGAGAA CATGGCTTTT 2760 TCTGAGACTA ATTTCCAAAG GCAGATTTTT TTTCCCCCAC AGGGAGTCCT CATTTCAAAA 2820 GGGCATGGTG TAGGGAAGCT TGACTGCAAC AACTTTCCCA TGGTAAATGT CATAGCGTGT 2880 TTTGTGTGGC TTTTCTTCTA GTGTTTTCTA TGCATATTGG GGGTAAACCC ACCAAACCTC 2940 CTGCAGTTCA GTAAAAGCAT TTGCGTGGAG GCCAGATTGA ATCTGAATTT TCCACTGTTC 3000 TGGTTTCATC AGGCCTAAAA TTTAGCAATA TCATATTGAG AGAAAGTAGG 3050
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