Variant report

Variant	rs6659158
Chromosome Location	chr1:173001063-173001064
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs1033465	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10465482	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10465506	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10732990	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10753068	1.00[ASN][1000 genomes]
rs10798248	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10798249	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10912514	0.86[EUR][1000 genomes]
rs1122312	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1159824	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1159825	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12025670	0.87[AMR][1000 genomes]
rs1467399	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1989627	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2092357	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2179426	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2206367	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2206368	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2206369	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2206370	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2206371	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2206372	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2206373	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2206375	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2206376	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2223520	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2223521	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2901695	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4916295	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6425193	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6425195	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6425196	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6425197	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6425198	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6659338	0.85[ASN][1000 genomes]
rs6661650	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6671875	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6681826	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6691232	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7416452	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7513007	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7516072	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7516980	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7518615	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7526839	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7528210	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7531129	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7531536	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7543619	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7549493	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7551105	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7552839	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7553670	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs960317	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs960318	0.86[EUR][1000 genomes];0.90[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	nsv831904	chr1:172912110-173070429	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv533953	chr1:172939335-173133255	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172995800-173008200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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