Variant report

Variant	rs6769642
Chromosome Location	chr3:160763469-160763470
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs1037888	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10513562	0.92[EUR][1000 genomes]
rs11708076	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12493960	0.93[ASN][1000 genomes]
rs13066683	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13098884	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1599374	0.93[ASN][1000 genomes]
rs1599376	0.93[ASN][1000 genomes]
rs1599383	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1599386	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1609688	0.93[ASN][1000 genomes]
rs1610158	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2306061	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2593812	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4273380	0.80[ASN][1000 genomes]
rs4342141	0.82[EUR][1000 genomes]
rs4370045	0.80[ASN][1000 genomes]
rs4414866	0.93[ASN][1000 genomes]
rs4597724	0.80[ASN][1000 genomes]
rs4616689	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4679671	0.92[EUR][1000 genomes]
rs4679926	0.81[EUR][1000 genomes]
rs5004752	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55672403	0.86[EUR][1000 genomes]
rs62280331	0.86[EUR][1000 genomes]
rs62280333	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6762645	0.80[ASN][1000 genomes]
rs6765269	0.80[ASN][1000 genomes]
rs6772578	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6774635	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6775627	0.80[ASN][1000 genomes]
rs6786871	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6806054	0.89[EUR][1000 genomes]
rs7615592	0.80[ASN][1000 genomes]
rs7619011	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7622047	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7623206	0.80[ASN][1000 genomes]
rs7628880	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7630674	0.86[AMR][1000 genomes]
rs7632423	0.91[EUR][1000 genomes]
rs7650703	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7653361	0.80[ASN][1000 genomes]
rs778642	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs778643	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs778645	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs778646	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs778648	0.84[EUR][1000 genomes]
rs778649	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs778653	0.89[EUR][1000 genomes]
rs778654	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs778657	0.89[EUR][1000 genomes]
rs778663	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs796609	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs898680	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs898681	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9290065	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs980975	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs980976	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9811594	0.92[EUR][1000 genomes]
rs9820825	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9831488	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9846756	0.80[ASN][1000 genomes]
rs9847866	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9848239	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9860360	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9875200	0.92[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	nsv931072	chr3:160669567-161159779	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 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	chr3:160745200-160782600	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr3:160760800-160767600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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