Variant report

Variant	rs1567036
Chromosome Location	chr4:97255608-97255609
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 166 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:158)

rs_ID	r²[population]
rs10002816	0.90[ASN][1000 genomes]
rs10006557	0.87[ASN][1000 genomes]
rs10007900	0.92[ASN][1000 genomes]
rs10009386	0.85[EUR][1000 genomes]
rs10010700	0.85[EUR][1000 genomes]
rs10015613	0.87[ASN][1000 genomes]
rs10016180	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs10021889	0.91[ASN][1000 genomes]
rs10032960	0.83[EUR][1000 genomes]
rs10213429	0.92[ASN][1000 genomes]
rs11097501	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11097502	0.92[ASN][1000 genomes]
rs11097505	0.92[ASN][1000 genomes]
rs11932384	0.80[ASN][1000 genomes]
rs11932562	0.85[EUR][1000 genomes]
rs11935830	0.85[ASN][1000 genomes]
rs12499067	0.82[ASN][1000 genomes]
rs12501360	0.89[ASN][1000 genomes]
rs12508802	0.90[ASN][1000 genomes]
rs12509883	0.92[ASN][1000 genomes]
rs12642471	0.82[ASN][1000 genomes]
rs12644982	0.80[ASN][1000 genomes]
rs12650441	0.88[ASN][1000 genomes]
rs13102896	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13104802	0.93[ASN][1000 genomes]
rs13121458	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13122821	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13122856	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13139267	0.85[EUR][1000 genomes]
rs13150508	0.92[ASN][1000 genomes]
rs1354704	0.91[ASN][1000 genomes]
rs1354706	0.91[ASN][1000 genomes]
rs1373331	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1395199	0.88[ASN][1000 genomes]
rs1400340	0.82[EUR][1000 genomes]
rs1425361	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1444021	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1506304	0.92[ASN][1000 genomes]
rs1506305	0.91[ASN][1000 genomes]
rs1506306	0.92[ASN][1000 genomes]
rs1506317	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1506318	0.90[ASN][1000 genomes]
rs1506319	0.92[ASN][1000 genomes]
rs1506320	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1506321	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1516671	0.84[EUR][1000 genomes]
rs1516673	0.85[EUR][1000 genomes]
rs1605227	0.91[ASN][1000 genomes]
rs17025493	0.82[ASN][1000 genomes]
rs1827888	0.85[EUR][1000 genomes]
rs1834360	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1847963	0.88[ASN][1000 genomes]
rs1847964	0.81[ASN][1000 genomes]
rs1847966	0.80[ASN][1000 genomes]
rs1847967	0.90[ASN][1000 genomes]
rs1847968	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1847969	1.00[CHB][hapmap];0.83[JPT][hapmap];0.92[ASN][1000 genomes]
rs1857889	0.88[ASN][1000 genomes]
rs1857890	0.93[ASN][1000 genomes]
rs1867400	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1911074	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1911076	0.92[ASN][1000 genomes]
rs1911077	0.91[ASN][1000 genomes]
rs1948912	0.84[ASN][1000 genomes]
rs2048022	0.92[ASN][1000 genomes]
rs2083922	0.90[ASN][1000 genomes]
rs2102786	0.85[EUR][1000 genomes]
rs2113973	0.80[ASN][1000 genomes]
rs2174584	0.91[ASN][1000 genomes]
rs2197322	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2203630	0.84[EUR][1000 genomes]
rs28407945	0.92[ASN][1000 genomes]
rs28523416	0.92[ASN][1000 genomes]
rs28565871	0.92[ASN][1000 genomes]
rs28633781	0.88[ASN][1000 genomes]
rs2865736	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28788633	0.92[ASN][1000 genomes]
rs35257138	0.89[ASN][1000 genomes]
rs36039803	0.90[ASN][1000 genomes]
rs4146410	0.84[ASN][1000 genomes]
rs4146411	0.84[ASN][1000 genomes]
rs4235424	0.84[EUR][1000 genomes]
rs4289448	0.85[EUR][1000 genomes]
rs4293790	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs4343731	0.82[ASN][1000 genomes]
rs4414959	0.88[ASN][1000 genomes]
rs4611939	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4613576	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4619895	0.92[ASN][1000 genomes]
rs4699283	0.86[ASN][1000 genomes]
rs4699285	0.92[ASN][1000 genomes]
rs4699287	0.90[ASN][1000 genomes]
rs4699288	0.86[ASN][1000 genomes]
rs4699485	0.82[ASN][1000 genomes]
rs4699496	0.86[ASN][1000 genomes]
rs4699501	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4699503	0.82[ASN][1000 genomes]
rs4699512	0.86[ASN][1000 genomes]
rs4699513	0.86[ASN][1000 genomes]
rs4699522	0.85[EUR][1000 genomes]
rs4699523	0.83[EUR][1000 genomes]
rs5017329	0.90[ASN][1000 genomes]
rs5017345	0.85[EUR][1000 genomes]
rs55680326	0.84[ASN][1000 genomes]
rs60275360	0.82[ASN][1000 genomes]
rs6419138	0.81[EUR][1000 genomes]
rs6532596	0.82[ASN][1000 genomes]
rs6532597	0.82[ASN][1000 genomes]
rs6532600	0.92[ASN][1000 genomes]
rs6532611	0.85[EUR][1000 genomes]
rs6532613	0.84[EUR][1000 genomes]
rs6532614	0.85[EUR][1000 genomes]
rs6532621	0.85[EUR][1000 genomes]
rs6815558	0.92[ASN][1000 genomes]
rs6815743	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6816447	0.92[ASN][1000 genomes]
rs6820075	0.82[ASN][1000 genomes]
rs6826156	0.82[ASN][1000 genomes]
rs6826365	0.85[EUR][1000 genomes]
rs6826478	0.84[EUR][1000 genomes]
rs6826817	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6830120	0.91[ASN][1000 genomes]
rs6831693	0.85[EUR][1000 genomes]
rs6831867	0.85[EUR][1000 genomes]
rs6832934	0.92[ASN][1000 genomes]
rs6835808	0.89[ASN][1000 genomes]
rs6836315	0.85[EUR][1000 genomes]
rs6837318	0.92[ASN][1000 genomes]
rs6841294	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6855768	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6857113	0.92[ASN][1000 genomes]
rs72883800	0.84[ASN][1000 genomes]
rs72885446	0.82[ASN][1000 genomes]
rs7435962	0.85[EUR][1000 genomes]
rs7653937	0.88[ASN][1000 genomes]
rs766061	0.88[ASN][1000 genomes]
rs7664054	0.85[EUR][1000 genomes]
rs7664279	0.81[EUR][1000 genomes]
rs7671604	0.88[ASN][1000 genomes]
rs7673756	0.91[ASN][1000 genomes]
rs7676317	0.82[ASN][1000 genomes]
rs7676764	0.82[ASN][1000 genomes]
rs7677339	0.85[EUR][1000 genomes]
rs7677553	0.85[EUR][1000 genomes]
rs7686174	0.91[ASN][1000 genomes]
rs7688727	0.85[EUR][1000 genomes]
rs7690397	0.90[ASN][1000 genomes]
rs9307167	0.92[ASN][1000 genomes]
rs9307168	0.92[ASN][1000 genomes]
rs931841	0.92[ASN][1000 genomes]
rs931842	0.92[ASN][1000 genomes]
rs938547	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs938548	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9683832	0.85[EUR][1000 genomes]
rs9884259	1.00[CHB][hapmap];0.85[JPT][hapmap];0.92[ASN][1000 genomes]
rs9884940	0.92[ASN][1000 genomes]
rs9998383	0.92[ASN][1000 genomes]
rs9999006	1.00[CHB][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470057	chr4:97104880-97311657	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv461589	chr4:97104881-97311657	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv594916	chr4:97104881-97311657	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv879631	chr4:97114706-97263153	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv879632	chr4:97118539-97308914	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv879633	chr4:97125086-97263153	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv461590	chr4:97197036-97266060	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv594917	chr4:97197036-97266060	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 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	chr4:97252400-97263200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links