Tag | Content |
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EnhancerAtlas ID | HS133-17400 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:102842890-102845020 |
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: 2 | Chromosome | Start | End |
chr2 | 102843334 | 102845009 | chr2 | 102844003 | 102844653 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I102226 | chr2 | 102842670 | 102846324 |
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Enhancer Sequence | GGAGAGGGAT GAGCTGCCTG CGGTTGGAGC TCTCTCTAGG CCCTGTACTT GGTGCCTGAA 60 GGGATTTAAG TCTTCAACTC TCAGATATGG AGAGAGATCA AACCAAGTTT GAATGTGACT 120 TCTCCACTTA CTCCCTATGT AAACTTAGAA AGATGTTTAA CTTTCTTCTA TTTCTCAGCT 180 ATAGAAAGGA ATAGAGGAAG GAAGGAAGGA GACAGGGAGG GAGGAAAGAA AGAGAGAGAG 240 AGGGAGGAAG GAAAGGAGAG AGGGAGGGAA AACGGAGGGA AGAAGGGAGT TTCGTAGAAA 300 AGAAACTAAA GAAAGCAGGG GAGAGAGATG GAGGAGAAGG GAGGAAGGGA AGAAAGAAGG 360 AAGGGAAGAA AAAAGAAAGA AACAAAGAAA GGGACAGTGA TTAAATCCTG CTTTTTGACA 420 GTGGGAATAA CTGAGTTGAA GTACAGGGAA GCATTCAGCG GGGCCTGGGC CACAGGGCGG 480 CCTCTATTGC TTGTCTGGAG GTCAAAACAA ATCCCCAACA CCACAGCTGT GGGTTTTAGT 540 CTGTGGGCCT ATGTCCTGCC AGTGCTGTTT GGCATAGAAA TGCCTCAGTG TGATCCTGAC 600 TCTCTGAGAG CCTGGCATTT CCCACCATGG TGCTTGTGAC TATGCTACTT TTGTTTTGTT 660 TTGTTTTGTT TTGTCTTAGA ACAGATACAA TCTATTAAGG CCTTGCAAAA GTAATAAATC 720 TGCTCTAAAG TCCCCTAATT AGATGAAAAA AGAAGCCTGG TGCAGCTGAT CTGTGTGGAG 780 ATGCACGACT TTATACCTTT TAAGTCCAGA GGCCTGAGTG ACAAGAGCAG GAAAGGGAGG 840 GAAACTGGTT GTCTGAGAAC GTTTTATGGG CCAGCTAAAA CATAAAAGAG GTCACTGGCA 900 TCAAGTGCTT GCTTTGCACA TAAAATACAC AGTACGGTTG TTGCCCACAT GTTTGATAAA 960 ACGTGGCTAT TCACTAACTT GGATTTTTTC CAAATTAAAT TTCTGAATTC AGAATTAGCA 1020 ACCCTGAGCA ATGTAGAAAG CGATAAACTC CTTTTTAATG ACAAAAGTCA TCTGAACCTT 1080 AAGTGTCCAG TGCAACCTGA AGTGCTGCTA GTACTGTGGA TAGTCCGACT GGGCATGGGG 1140 AGGGGGTCTC TGGTTTTGGC TCTGGCATCT GCAGAGGCCG CCCCGTCTAA GCACACCCAT 1200 GACTGCTCTC TCCTGCTTGC GTCTTTGAGA AGAAGACAGT TCAGTCCCCC ACCACTGATT 1260 GTTTTCTGAC ACAGAGTTGA GTGGTTCAGT TGCTTTCTAC TTTTTGACTA ACAGAAGCCT 1320 GCGTCACTTT ACGTATTCTT CCTGGAAGCT CAGGCCCCAT GGTGTGTCTC TCTCACTGTC 1380 TCTCTCTCTC ACTGACTCTG TCAGTGACTC TCTCACTGAG TCATTGCGAC TCCCAGGAGC 1440 GTGACTATAG CTGTGACTTA TGGGTGTTGT GCAGTGTGTG GGGAAGCTGC TAGTGAGGTC 1500 GAGTTTAGCA GGAAGAGAAA ACAGGAATAG TGACTCACAC GGAGTAGTGG GGGCTGGGCA 1560 GATGAGAGAG TTAGGCAGCC CCGCCCTCTG CTGAGACTGG GACGCAGCCC AGATTCTGCA 1620 ACAGTGGGCA GAGGATTTGG CGATGGAGGC TAACAGGCAG CCAGGGGTCC TTTTTTTCTT 1680 TATTTTTATT TTGCTTAATT CAGAAAAGTA TGTGTGCATT TTGTGATGAA ATTCTCTACA 1740 GCTCTGTCTA CGAGAACTGC CCTGTAATAT CTCTGTGTGT TGGCTTTAAC AGTGAGCTAC 1800 TGATGAGATT CTGAGATTAG TCCCAGATCT TGTTTATGTC CTTGTTCCCC TTGAGGATAT 1860 TTTCTGAGTT AAATCAGGAA ATACCGATTA ATGGATGAAA ATGAGAAAGA GAGAAATAAT 1920 GTCCTTCGTA GGATAAGTCA TTTACCCTGA CTAGGTTAGC TAAGCTGTAT CACTCAATTA 1980 ATAATTAGGT GTGCATGACT CACCATTTTA GAAGGAGCCA TTGACAGCCC TAGCTGAAGT 2040 CAGCAAGTTC TGTATCTTCT CTAGCAAGCC ACTGGAGCTT TACAAATTCT CCTGGCAGGG 2100 GTGCATGTGT GTACGAGGAT GGAAGGGTCT 2130
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