Variant report

Variant	rs2852970
Chromosome Location	chr18:45284314-45284315
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1004765	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1107933	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1107934	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1466905	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1579118	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1604556	0.89[EUR][1000 genomes]
rs1894150	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1910235	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1995413	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2097175	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2134374	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2174028	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2653629	0.86[EUR][1000 genomes]
rs2653630	0.92[EUR][1000 genomes]
rs2653632	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2653633	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2653634	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2653635	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2653636	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2653637	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2653638	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2653639	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2653641	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2653642	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2653643	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2653644	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2653645	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2653647	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2653648	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2653651	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2653652	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2653653	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2653654	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2653655	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2653656	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2653657	0.83[EUR][1000 genomes]
rs2852942	0.87[ASN][1000 genomes]
rs2852949	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2852950	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2852952	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2852954	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2852958	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2852960	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2852961	0.90[EUR][1000 genomes]
rs2852965	0.85[AFR][1000 genomes]
rs2852966	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2852967	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2852969	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62086466	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs877354	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9954192	0.85[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	esv3425854	chr18:45188942-45336590	Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45282800-45300600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr18:45284200-45284600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr18:45284200-45284800	Weak transcription	Gastric	stomach

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