Variant report

Variant	rs2923637
Chromosome Location	chr8:34966389-34966390
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10503969	1.00[ASN][1000 genomes]
rs10503970	1.00[ASN][1000 genomes]
rs10808338	1.00[ASN][1000 genomes]
rs10954974	1.00[ASN][1000 genomes]
rs11774088	1.00[ASN][1000 genomes]
rs11779612	1.00[ASN][1000 genomes]
rs11782611	1.00[ASN][1000 genomes]
rs11785346	1.00[ASN][1000 genomes]
rs1376517	1.00[ASN][1000 genomes]
rs17249248	1.00[ASN][1000 genomes]
rs17249529	1.00[ASN][1000 genomes]
rs17250409	1.00[ASN][1000 genomes]
rs2012407	1.00[ASN][1000 genomes]
rs2218870	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2405530	1.00[ASN][1000 genomes]
rs2923630	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2923631	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2923632	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2923636	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2923638	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2923639	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2923640	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2923641	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2923663	1.00[ASN][1000 genomes]
rs2981315	1.00[ASN][1000 genomes]
rs2981330	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981331	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981332	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981342	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2981356	1.00[ASN][1000 genomes]
rs4269538	1.00[ASN][1000 genomes]
rs4351412	1.00[ASN][1000 genomes]
rs4527864	1.00[ASN][1000 genomes]
rs4535735	1.00[ASN][1000 genomes]
rs56821785	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62505637	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62505639	1.00[ASN][1000 genomes]
rs62505640	1.00[ASN][1000 genomes]
rs6468305	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6986169	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7011522	1.00[ASN][1000 genomes]
rs7460698	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017085	chr8:34742896-35594241	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv539546	chr8:34742896-35594241	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr8:34964800-34966600	Enhancers	Liver	Liver
2	chr8:34966200-34967800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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