Variant report

Variant	rs1567491
Chromosome Location	chr4:127912724-127912725
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:127875714..127878678-chr4:127910888..127914676,3	K562	blood:

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10014196	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1021062	0.81[ASN][1000 genomes]
rs11098905	0.85[ASN][1000 genomes]
rs11098911	0.81[ASN][1000 genomes]
rs1155256	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11721464	0.86[ASN][1000 genomes]
rs11723741	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11723829	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11734026	0.84[ASN][1000 genomes]
rs11736547	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12502193	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12504419	0.86[ASN][1000 genomes]
rs12508997	0.86[ASN][1000 genomes]
rs12509001	0.86[ASN][1000 genomes]
rs12510422	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12512914	0.86[ASN][1000 genomes]
rs13101381	0.84[ASN][1000 genomes]
rs13101547	0.88[EUR][1000 genomes]
rs13107386	0.86[ASN][1000 genomes]
rs13107479	0.84[ASN][1000 genomes]
rs13111315	0.86[ASN][1000 genomes]
rs13123992	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13125496	0.80[ASN][1000 genomes]
rs13138236	0.86[ASN][1000 genomes]
rs13141720	0.85[ASN][1000 genomes]
rs1397433	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1510680	0.88[EUR][1000 genomes]
rs1533089	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17011876	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17011922	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17011977	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1877072	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1995904	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1995906	0.85[ASN][1000 genomes]
rs1995907	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2048379	0.84[ASN][1000 genomes]
rs2219924	0.81[ASN][1000 genomes]
rs2221774	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34597806	0.86[ASN][1000 genomes]
rs34872217	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4146424	0.81[ASN][1000 genomes]
rs4833360	0.82[ASN][1000 genomes]
rs4833362	0.86[ASN][1000 genomes]
rs4833366	0.85[ASN][1000 genomes]
rs4834154	0.82[ASN][1000 genomes]
rs4834155	0.82[ASN][1000 genomes]
rs4834161	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56280971	0.84[ASN][1000 genomes]
rs60923968	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6534592	0.84[ASN][1000 genomes]
rs67251456	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6814753	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6833994	0.81[ASN][1000 genomes]
rs6834065	0.81[ASN][1000 genomes]
rs6837327	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6848070	0.86[ASN][1000 genomes]
rs7667742	0.90[EUR][1000 genomes]
rs7680252	0.84[ASN][1000 genomes]
rs7685181	0.86[ASN][1000 genomes]
rs925374	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs989212	0.81[ASN][1000 genomes]
rs9942226	0.86[ASN][1000 genomes]
rs997404	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428773	chr4:127760014-127913973	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv830055	chr4:127794875-127993821	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv879913	chr4:127844803-127948196	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	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	chr4:127908200-127913000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:127912600-127914800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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