Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10494931	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10494932	0.90[ASN][1000 genomes]
rs11119658	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11119664	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11578692	0.86[ASN][1000 genomes]
rs11579078	0.86[ASN][1000 genomes]
rs11582507	0.90[ASN][1000 genomes]
rs11583101	0.90[ASN][1000 genomes]
rs11588573	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12074568	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12722738	0.92[ASN][1000 genomes]
rs12750762	0.86[ASN][1000 genomes]
rs12751504	0.83[ASN][1000 genomes]
rs12752336	0.83[ASN][1000 genomes]
rs12756697	0.90[ASN][1000 genomes]
rs12760791	0.90[ASN][1000 genomes]
rs1393028	0.90[ASN][1000 genomes]
rs17188797	0.86[ASN][1000 genomes]
rs2221250	0.94[ASN][1000 genomes]
rs33985151	0.83[ASN][1000 genomes]
rs35019263	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4262610	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4638187	0.86[ASN][1000 genomes]
rs59374111	0.94[ASN][1000 genomes]
rs61850226	0.90[ASN][1000 genomes]
rs6669457	0.94[AFR][1000 genomes]
rs6702598	0.86[ASN][1000 genomes]
rs7414286	0.86[ASN][1000 genomes]
rs7519090	0.90[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	nsv4410	chr1:211193724-211210571	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211182800-211228600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:211192600-211209000	Weak transcription	HSMMtube	muscle
3	chr1:211194400-211209200	Weak transcription	HSMM	muscle
4	chr1:211198800-211209600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:211199800-211200200	Enhancers	Brain Substantia Nigra	brain

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