Variant report

Variant	rs11716632
Chromosome Location	chr3:56193660-56193661
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	chr3:56188195..56189971-chr3:56191874..56194144,2	K562	blood:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10433552	0.82[EUR][1000 genomes]
rs10433620	0.82[EUR][1000 genomes]
rs11130503	0.81[EUR][1000 genomes]
rs11709589	0.81[EUR][1000 genomes]
rs11712407	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11716452	0.83[EUR][1000 genomes]
rs11917679	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12636541	0.83[EUR][1000 genomes]
rs13061788	0.81[EUR][1000 genomes]
rs13070314	0.81[EUR][1000 genomes]
rs13084765	0.81[EUR][1000 genomes]
rs13087905	0.82[EUR][1000 genomes]
rs13096822	0.82[EUR][1000 genomes]
rs13097517	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13097694	0.82[EUR][1000 genomes]
rs13100274	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1376980	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1376983	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1452216	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1485678	0.80[EUR][1000 genomes]
rs1901553	0.81[EUR][1000 genomes]
rs1994294	0.81[EUR][1000 genomes]
rs2316475	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2316476	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2316484	0.82[EUR][1000 genomes]
rs28823346	0.83[EUR][1000 genomes]
rs34235403	0.81[EUR][1000 genomes]
rs35138614	0.82[EUR][1000 genomes]
rs4318528	0.82[EUR][1000 genomes]
rs4974119	0.83[EUR][1000 genomes]
rs4974181	0.82[EUR][1000 genomes]
rs4974184	0.81[EUR][1000 genomes]
rs6445771	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6445773	0.81[EUR][1000 genomes]
rs6445774	0.81[EUR][1000 genomes]
rs6764950	0.83[EUR][1000 genomes]
rs6805098	0.80[EUR][1000 genomes]
rs7628015	0.82[EUR][1000 genomes]
rs7633985	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9311598	0.83[EUR][1000 genomes]
rs982477	0.82[EUR][1000 genomes]
rs991334	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009709	chr3:56000827-56294945	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr3:56192400-56204200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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