Variant report

Variant	rs11742568
Chromosome Location	chr5:68360310-68360311
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10036073	0.81[ASN][1000 genomes]
rs10078240	0.82[ASN][1000 genomes]
rs10471766	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10940194	0.81[ASN][1000 genomes]
rs11744305	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12108990	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12651824	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs164795	0.84[ASN][1000 genomes]
rs164796	0.84[ASN][1000 genomes]
rs164798	0.84[ASN][1000 genomes]
rs164801	0.82[ASN][1000 genomes]
rs164802	0.82[ASN][1000 genomes]
rs186832	0.84[ASN][1000 genomes]
rs2076823	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2130758	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2327640	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2434352	0.84[ASN][1000 genomes]
rs2450236	0.84[ASN][1000 genomes]
rs2450237	0.84[ASN][1000 genomes]
rs338676	0.84[ASN][1000 genomes]
rs338677	0.84[ASN][1000 genomes]
rs3923114	0.82[ASN][1000 genomes]
rs4246762	0.81[ASN][1000 genomes]
rs4246763	0.81[ASN][1000 genomes]
rs4295341	0.82[ASN][1000 genomes]
rs4315885	0.81[ASN][1000 genomes]
rs4410610	0.81[ASN][1000 genomes]
rs4976063	0.81[ASN][1000 genomes]
rs4976075	0.81[ASN][1000 genomes]
rs4976076	0.81[ASN][1000 genomes]
rs4976178	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56198247	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56205286	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56238212	0.82[ASN][1000 genomes]
rs60544415	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62354528	0.81[ASN][1000 genomes]
rs62372624	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6450003	0.82[ASN][1000 genomes]
rs6450015	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6450016	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6450018	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6874442	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6879036	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6893702	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7444785	0.81[ASN][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	nsv968920	chr5:68350235-68371417	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 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	chr5:68360200-68370200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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