Variant report

Variant	rs17511324
Chromosome Location	chr4:19697730-19697731
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10516335	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11721854	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11721864	0.83[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11722812	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11930962	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11936583	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11939339	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11942433	0.83[EUR][1000 genomes]
rs17508080	0.81[AFR][1000 genomes]
rs17511289	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17511721	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17570085	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs17570168	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs2200748	0.81[AFR][1000 genomes]
rs28629819	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4593130	0.81[AFR][1000 genomes]
rs56182249	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62295090	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62295099	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62295100	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62295102	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62295104	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62295107	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62295108	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62295139	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62295151	0.87[ASN][1000 genomes]
rs62295153	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62296261	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62296262	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62296264	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62296266	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62296271	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62296887	0.91[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs62296905	0.83[EUR][1000 genomes]
rs6846330	0.81[AFR][1000 genomes]
rs6846645	0.81[AFR][1000 genomes]
rs6848523	0.91[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs6853029	0.83[EUR][1000 genomes]
rs73236204	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73249357	0.81[AFR][1000 genomes]
rs73249365	0.81[AFR][1000 genomes]
rs73249369	0.81[AFR][1000 genomes]
rs73249379	0.81[AFR][1000 genomes]
rs73249381	0.81[AFR][1000 genomes]
rs7665257	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7666136	0.90[AFR][1000 genomes]
rs7667493	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7675318	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7682588	0.81[AFR][1000 genomes]
rs901927	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878733	chr4:19335464-19928602	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv461286	chr4:19488871-19709795	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv593786	chr4:19488871-19709795	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv829873	chr4:19582263-19742515	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv829874	chr4:19635213-19781102	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv529290	chr4:19658583-20173839	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr4:19696800-19697800	Enhancers	Primary hematopoietic stem cells	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links