Variant report

Variant	rs13339777
Chromosome Location	chr2:167977532-167977533
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10497314	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10497315	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11899616	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11899748	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11900038	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12105903	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs12619579	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1346723	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1429930	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs2390513	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56730065	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs56836723	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59272620	0.80[AMR][1000 genomes]
rs59632215	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59877654	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61084716	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs6432973	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6432974	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6432975	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6432976	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6432977	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6706173	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6743737	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs68091366	0.83[EUR][1000 genomes]
rs7557440	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7572454	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7580360	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs7588368	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7606905	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs7607028	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs9967718	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[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	nsv875376	chr2:167844513-168037489	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region 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	chr2:167973000-167978200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:167973200-167978000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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