Variant report

Variant	rs1203342
Chromosome Location	chr6:130870469-130870470
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10872372	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1203340	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1203341	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1203343	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1203344	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1203345	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1203346	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1203347	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1203348	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12526873	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1316493	0.80[EUR][1000 genomes]
rs1316537	0.80[EUR][1000 genomes]
rs1316538	0.80[EUR][1000 genomes]
rs1317232	0.80[EUR][1000 genomes]
rs1933757	0.80[EUR][1000 genomes]
rs1933759	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1933764	0.96[ASN][1000 genomes]
rs1933765	0.96[ASN][1000 genomes]
rs1933766	0.96[ASN][1000 genomes]
rs1933767	0.95[ASN][1000 genomes]
rs1933768	0.96[ASN][1000 genomes]
rs2326916	0.91[ASN][1000 genomes]
rs2876084	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4144216	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4895886	0.81[EUR][1000 genomes]
rs4895887	0.80[EUR][1000 genomes]
rs4897429	0.96[ASN][1000 genomes]
rs4897437	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs6569688	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6569690	0.81[EUR][1000 genomes]
rs6932172	0.84[EUR][1000 genomes]
rs6932344	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6940599	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs766966	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs766967	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7744825	0.80[EUR][1000 genomes]
rs7768049	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9321230	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9321238	0.91[CEU][hapmap];0.80[EUR][1000 genomes]
rs9321239	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs9321241	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs9372966	0.81[EUR][1000 genomes]
rs9372967	0.80[EUR][1000 genomes]
rs9375731	0.96[ASN][1000 genomes]
rs9375740	0.81[EUR][1000 genomes]
rs9375741	0.81[EUR][1000 genomes]
rs9388802	0.96[ASN][1000 genomes]
rs9402246	0.81[EUR][1000 genomes]
rs9402247	0.81[EUR][1000 genomes]
rs9402248	0.80[EUR][1000 genomes]
rs9483145	0.80[EUR][1000 genomes]
rs9492649	0.80[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	nsv533971	chr6:130490694-131172051	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 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	chr6:130869400-130872800	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr6:130869400-130873000	Weak transcription	Skeletal Muscle Male	skeletal muscle

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