Variant report

Variant	rs4693219
Chromosome Location	chr4:90005589-90005590
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10001420	0.80[AMR][1000 genomes]
rs11734924	0.88[AMR][1000 genomes]
rs12647095	0.83[AMR][1000 genomes]
rs12649875	0.88[AMR][1000 genomes]
rs13133608	0.88[AMR][1000 genomes]
rs1355836	0.90[AMR][1000 genomes]
rs1355837	0.85[AMR][1000 genomes]
rs1398937	0.85[AMR][1000 genomes]
rs1398938	0.80[AMR][1000 genomes]
rs1398939	0.80[AMR][1000 genomes]
rs1398941	0.80[AMR][1000 genomes]
rs1398943	0.81[AMR][1000 genomes]
rs1513812	0.90[AMR][1000 genomes]
rs1513823	0.85[AMR][1000 genomes]
rs1533288	0.85[AMR][1000 genomes]
rs1533289	0.90[AMR][1000 genomes]
rs1708659	0.85[AMR][1000 genomes]
rs1708671	0.85[AMR][1000 genomes]
rs1708672	0.80[AMR][1000 genomes]
rs1708683	0.85[AMR][1000 genomes]
rs1795730	0.80[AMR][1000 genomes]
rs1795735	0.85[AMR][1000 genomes]
rs1795740	0.80[AMR][1000 genomes]
rs1828735	0.85[AMR][1000 genomes]
rs1996139	0.90[AMR][1000 genomes]
rs2056013	0.90[AMR][1000 genomes]
rs2102650	0.95[AMR][1000 genomes]
rs2670618	0.85[AMR][1000 genomes]
rs2670619	0.80[AMR][1000 genomes]
rs2670620	0.80[AMR][1000 genomes]
rs2670627	0.85[AMR][1000 genomes]
rs2670628	0.85[AMR][1000 genomes]
rs2704580	0.85[AMR][1000 genomes]
rs2704585	0.85[AMR][1000 genomes]
rs2704592	0.83[AMR][1000 genomes]
rs2869989	0.95[AMR][1000 genomes]
rs28718401	0.85[AMR][1000 genomes]
rs28869547	0.80[AMR][1000 genomes]
rs2904264	0.95[AMR][1000 genomes]
rs4693984	0.88[AMR][1000 genomes]
rs6532100	0.85[AMR][1000 genomes]
rs6823241	0.88[AMR][1000 genomes]
rs6826482	0.95[AMR][1000 genomes]
rs6834297	0.90[AMR][1000 genomes]
rs6845264	0.95[AMR][1000 genomes]
rs7657630	0.88[AMR][1000 genomes]
rs8180333	0.85[AMR][1000 genomes]
rs9307063	0.88[AMR][1000 genomes]
rs938265	0.90[AMR][1000 genomes]
rs938267	0.88[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470051	chr4:89644931-90643144	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1007025	chr4:89837734-90098046	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv537176	chr4:89837734-90098046	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1002448	chr4:89933385-90128133	Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:89996400-90009800	Weak transcription	Pancreas	Pancrea

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