Variant report
Variant | rs17538138 |
---|---|
Chromosome Location | chr2:208934033-208934034 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr2:208926513..208930859-chr2:208931530..208934190,4 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10192860 | 0.88[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs10497895 | 1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs10932224 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs12464255 | 1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs12465052 | 1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs12465292 | 0.85[CEU][hapmap];1.00[YRI][hapmap] |
rs12470702 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs13428099 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs13431014 | 0.85[CEU][hapmap] |
rs16840403 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs17459574 | 1.00[YRI][hapmap] |
rs17459758 | 0.85[CEU][hapmap];1.00[YRI][hapmap] |
rs17538061 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs2362787 | 0.91[EUR][1000 genomes] |
rs57709782 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs60335988 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs62192772 | 0.88[EUR][1000 genomes] |
rs62192773 | 0.88[EUR][1000 genomes] |
rs62192790 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs62192791 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs62192812 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs62192814 | 0.95[EUR][1000 genomes] |
rs62192815 | 0.95[EUR][1000 genomes] |
rs62192816 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs62192818 | 0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs6435402 | 0.85[CEU][hapmap] |
rs6740362 | 0.85[CEU][hapmap] |
rs72981543 | 0.93[EUR][1000 genomes] |
rs72984907 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72984917 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs72984926 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72984930 | 0.94[EUR][1000 genomes] |
rs72984932 | 0.94[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1010531 | chr2:208610639-209176782 | Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
2 | nsv536130 | chr2:208610639-209176782 | Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
3 | nsv875743 | chr2:208688648-208940023 | Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
4 | nsv534496 | chr2:208814372-209302791 | Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:208933600-208934400 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
2 | chr2:208933800-208934200 | Enhancers | HSMM | muscle |