Variant report

Variant	rs4375930
Chromosome Location	chr20:40850522-40850523
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs1014757	0.94[EUR][1000 genomes]
rs11907691	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11907769	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12625238	0.93[EUR][1000 genomes]
rs13040788	0.89[EUR][1000 genomes]
rs16986670	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1883376	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1883377	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1984399	0.85[ASN][1000 genomes]
rs2143632	0.94[EUR][1000 genomes]
rs2223426	0.84[EUR][1000 genomes]
rs2223718	0.91[EUR][1000 genomes]
rs2867063	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2903465	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6016705	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6016706	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6016707	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6016708	0.84[EUR][1000 genomes]
rs6016709	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6016710	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6016711	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6016712	0.88[EUR][1000 genomes]
rs6016713	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6016722	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6030018	0.81[EUR][1000 genomes]
rs6030023	0.83[EUR][1000 genomes]
rs6030026	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6030027	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6030029	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6030035	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6030036	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6030037	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6030058	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6030061	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6030069	0.91[ASN][1000 genomes]
rs6030072	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6030073	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6030084	0.84[ASN][1000 genomes]
rs6030089	0.87[ASN][1000 genomes]
rs6030101	0.81[ASN][1000 genomes]
rs6065451	0.87[ASN][1000 genomes]
rs6072672	0.87[ASN][1000 genomes]
rs6093584	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6093588	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6093589	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6093595	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6093598	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6102704	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6102713	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6102714	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6124427	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6124429	0.93[EUR][1000 genomes]
rs6124435	0.82[ASN][1000 genomes]
rs6130062	0.80[EUR][1000 genomes]
rs6130068	0.83[EUR][1000 genomes]
rs6130071	0.85[EUR][1000 genomes]
rs6130073	0.89[EUR][1000 genomes]
rs6130074	0.88[EUR][1000 genomes]
rs6130076	0.90[EUR][1000 genomes]
rs6130081	0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6130091	0.84[ASN][1000 genomes]
rs6513772	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7270492	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs727336	0.88[ASN][1000 genomes]
rs728373	0.89[ASN][1000 genomes]
rs728374	0.89[ASN][1000 genomes]
rs742290	0.82[AMR][1000 genomes];0.89[EUR][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	esv2751913	chr20:40422982-41269321	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv532516	chr20:40451059-41097155	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 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	chr20:40850400-40851800	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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