Variant report

Variant	rs35049898
Chromosome Location	chr2:181982277-181982278
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11891215	0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11893821	0.89[EUR][1000 genomes]
rs12999974	0.89[EUR][1000 genomes]
rs13011751	0.82[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs13012524	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs13020845	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs13025711	0.86[EUR][1000 genomes]
rs13033467	0.88[EUR][1000 genomes]
rs34601234	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34714467	0.89[EUR][1000 genomes]
rs35323141	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35543145	0.89[EUR][1000 genomes]
rs55664819	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55900432	0.89[EUR][1000 genomes]
rs55954384	0.89[EUR][1000 genomes]
rs56169464	0.86[EUR][1000 genomes]
rs59395276	0.86[EUR][1000 genomes]
rs62178846	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6433892	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6433895	0.86[EUR][1000 genomes]
rs6706397	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6706696	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6710650	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6711938	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6746347	0.89[EUR][1000 genomes]
rs6759865	0.88[EUR][1000 genomes]
rs7558428	0.89[EUR][1000 genomes]
rs7566146	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7566256	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7566434	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7569991	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7580796	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7592486	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7598960	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431824	chr2:181946115-182118559	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1005870	chr2:181968637-182921439	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv536063	chr2:181968637-182921439	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv459954	chr2:181975252-182040293	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv583910	chr2:181975252-182040293	ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:181973800-181985000	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr2:181974000-181985200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr2:181980800-181982800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr2:181981000-181985000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr2:181981400-181982400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr2:181981400-181984800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr2:181981400-181988600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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