Variant report

Variant	rs2351675
Chromosome Location	chr8:63274057-63274058
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10504345	0.91[ASN][1000 genomes]
rs10504346	0.91[ASN][1000 genomes]
rs13267288	0.91[ASN][1000 genomes]
rs1349557	0.84[ASN][1000 genomes]
rs1349558	0.84[ASN][1000 genomes]
rs16928745	0.93[ASN][1000 genomes]
rs16928749	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16928771	0.90[ASN][1000 genomes]
rs16928779	0.91[ASN][1000 genomes]
rs16928780	0.89[ASN][1000 genomes]
rs16928781	0.88[ASN][1000 genomes]
rs16928784	0.91[ASN][1000 genomes]
rs16928822	0.91[ASN][1000 genomes]
rs16928835	0.91[ASN][1000 genomes]
rs16928842	0.91[ASN][1000 genomes]
rs16928845	0.91[ASN][1000 genomes]
rs16928847	0.91[ASN][1000 genomes]
rs16928852	0.91[ASN][1000 genomes]
rs16928856	0.91[ASN][1000 genomes]
rs16928857	0.91[ASN][1000 genomes]
rs16928883	0.84[ASN][1000 genomes]
rs16928887	0.82[ASN][1000 genomes]
rs16928889	0.82[ASN][1000 genomes]
rs16928891	0.82[ASN][1000 genomes]
rs16928902	0.82[ASN][1000 genomes]
rs16928904	0.82[ASN][1000 genomes]
rs16928919	0.82[ASN][1000 genomes]
rs16928922	0.82[ASN][1000 genomes]
rs1973021	0.80[ASN][1000 genomes]
rs2123037	0.84[ASN][1000 genomes]
rs2351667	0.96[AFR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4379439	0.93[ASN][1000 genomes]
rs4738963	0.91[ASN][1000 genomes]
rs4738964	0.91[ASN][1000 genomes]
rs4738965	0.90[ASN][1000 genomes]
rs4738966	0.91[ASN][1000 genomes]
rs4738967	0.91[ASN][1000 genomes]
rs4738968	0.91[ASN][1000 genomes]
rs4738969	0.91[ASN][1000 genomes]
rs56769034	0.91[ASN][1000 genomes]
rs56995369	0.91[ASN][1000 genomes]
rs57800177	0.82[ASN][1000 genomes]
rs57875814	0.91[ASN][1000 genomes]
rs58313700	0.91[ASN][1000 genomes]
rs58534646	0.98[ASN][1000 genomes]
rs58756888	0.91[ASN][1000 genomes]
rs59620803	0.91[ASN][1000 genomes]
rs60193051	0.91[ASN][1000 genomes]
rs60235230	0.91[ASN][1000 genomes]
rs60421957	0.85[ASN][1000 genomes]
rs60500327	0.91[ASN][1000 genomes]
rs60536390	0.82[ASN][1000 genomes]
rs61318422	0.91[ASN][1000 genomes]
rs62509191	0.98[ASN][1000 genomes]
rs62509192	0.98[ASN][1000 genomes]
rs62509193	0.91[ASN][1000 genomes]
rs62509209	0.91[ASN][1000 genomes]
rs62509210	0.91[ASN][1000 genomes]
rs62509211	0.91[ASN][1000 genomes]
rs62509212	0.91[ASN][1000 genomes]
rs62509213	0.90[ASN][1000 genomes]
rs62509214	0.91[ASN][1000 genomes]
rs62509215	0.91[ASN][1000 genomes]
rs62509216	0.91[ASN][1000 genomes]
rs62509219	0.88[ASN][1000 genomes]
rs62509220	0.91[ASN][1000 genomes]
rs62509223	0.91[ASN][1000 genomes]
rs62509224	0.91[ASN][1000 genomes]
rs62509244	0.89[ASN][1000 genomes]
rs62509246	0.91[ASN][1000 genomes]
rs62509248	0.90[ASN][1000 genomes]
rs62509249	0.90[ASN][1000 genomes]
rs62509250	0.86[ASN][1000 genomes]
rs62509251	0.85[ASN][1000 genomes]
rs62509254	0.84[ASN][1000 genomes]
rs62509255	0.82[ASN][1000 genomes]
rs62509256	0.84[ASN][1000 genomes]
rs62509258	0.81[ASN][1000 genomes]
rs7014811	0.93[AFR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72505477	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019143	chr8:63142202-63390820	Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv890956	chr8:63251640-63346420	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv890957	chr8:63266645-63310921	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63272200-63275200	Enhancers	HMEC	breast
2	chr8:63272400-63276000	Enhancers	Muscle Satellite Cultured Cells	--
3	chr8:63272800-63274600	Enhancers	A549	lung
4	chr8:63273800-63275000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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