Variant report

Variant	rs7559968
Chromosome Location	chr2:50225812-50225813
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs10495991	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10495992	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10495993	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10495994	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1159136	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1159137	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11887101	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11889551	0.85[AMR][1000 genomes]
rs11896576	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11896677	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11899849	0.82[AMR][1000 genomes]
rs12615365	0.85[AMR][1000 genomes]
rs12620898	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1363025	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1363038	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1369294	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1421582	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1421583	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1421584	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1421585	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17440201	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17441066	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17441242	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17441396	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17493081	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17493116	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17493390	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17493439	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17494124	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1865488	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1865489	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1895126	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1895127	0.85[AMR][1000 genomes]
rs1895129	0.85[AMR][1000 genomes]
rs2112073	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2193866	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2193867	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2216522	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2351146	0.85[AMR][1000 genomes]
rs2351148	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2882594	0.85[AMR][1000 genomes]
rs3796036	0.83[AMR][1000 genomes]
rs4404319	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs57193820	0.83[AMR][1000 genomes]
rs57707897	0.85[AMR][1000 genomes]
rs58564477	0.82[AMR][1000 genomes]
rs59032342	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs59781568	0.85[AMR][1000 genomes]
rs60267441	0.80[AMR][1000 genomes]
rs61073961	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61405508	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs62132489	0.83[AMR][1000 genomes]
rs62132490	0.82[AMR][1000 genomes]
rs62134599	0.81[AMR][1000 genomes]
rs62134600	0.85[AMR][1000 genomes]
rs62134607	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs62134608	0.82[AMR][1000 genomes]
rs62134651	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs62134654	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62134655	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62134656	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62134657	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6545142	0.80[EUR][1000 genomes]
rs6710767	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6719571	0.85[AMR][1000 genomes]
rs6733024	0.90[ASN][1000 genomes]
rs6747457	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs72887815	0.85[AMR][1000 genomes]
rs72887817	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs72887819	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72887820	0.84[AMR][1000 genomes]
rs72887870	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72887883	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7426139	0.83[AMR][1000 genomes]
rs7563039	0.85[AMR][1000 genomes]
rs7563354	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7565688	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7565706	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7569617	0.82[AMR][1000 genomes]
rs7573338	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7573588	0.80[EUR][1000 genomes]
rs7587669	0.81[AMR][1000 genomes]
rs7590237	0.84[AMR][1000 genomes]
rs7591097	0.82[AMR][1000 genomes]
rs7595904	0.84[AMR][1000 genomes]
rs7599940	0.84[AMR][1000 genomes]
rs7603788	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9941548	0.87[AMR][1000 genomes];0.82[EUR][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	esv3388948	chr2:50092667-50602681	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
2	esv3399511	chr2:50092687-50602651	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv934303	chr2:50145598-50412189	Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
4	nsv874031	chr2:50202953-50243386	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50223400-50233000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:50225800-50226200	Enhancers	H1 Cell Line	embryonic stem cell

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