Variant report

Variant	rs73608267
Chromosome Location	chr10:25588912-25588913
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1413400	0.94[ASN][1000 genomes]
rs1416993	0.94[ASN][1000 genomes]
rs1416994	0.94[ASN][1000 genomes]
rs16925561	0.84[ASN][1000 genomes]
rs55801305	0.94[ASN][1000 genomes]
rs56084254	0.91[ASN][1000 genomes]
rs56257605	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs58585465	0.94[ASN][1000 genomes]
rs58942965	0.94[ASN][1000 genomes]
rs58968345	0.86[ASN][1000 genomes]
rs59521850	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60268096	0.94[ASN][1000 genomes]
rs60352386	0.91[ASN][1000 genomes]
rs60876342	0.86[ASN][1000 genomes]
rs61082972	0.94[ASN][1000 genomes]
rs61105987	0.91[ASN][1000 genomes]
rs61108946	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61271645	0.86[ASN][1000 genomes]
rs61530525	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs66463292	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs66539540	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs66810403	0.94[ASN][1000 genomes]
rs66924755	0.91[ASN][1000 genomes]
rs66963587	0.94[ASN][1000 genomes]
rs67069034	0.94[ASN][1000 genomes]
rs67389824	0.94[ASN][1000 genomes]
rs67675896	0.94[ASN][1000 genomes]
rs67709672	0.89[ASN][1000 genomes]
rs67733590	0.94[ASN][1000 genomes]
rs67963266	0.91[ASN][1000 genomes]
rs67969515	0.91[ASN][1000 genomes]
rs68159928	0.94[ASN][1000 genomes]
rs7093650	0.94[ASN][1000 genomes]
rs7093651	0.94[ASN][1000 genomes]
rs7093692	0.94[ASN][1000 genomes]
rs72792092	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72794261	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73608266	0.94[ASN][1000 genomes]
rs74123822	0.82[ASN][1000 genomes]
rs74123863	0.84[ASN][1000 genomes]
rs74126521	0.85[ASN][1000 genomes]
rs7476751	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7904501	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9663151	0.86[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	esv2761583	chr10:25525657-25722444	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25582000-25592000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr10:25588800-25589400	Enhancers	Sigmoid Colon	Sigmoid Colon
3	chr10:25588800-25589600	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr10:25588800-25589800	Enhancers	HUES6 Cell Line	embryonic stem cell

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