Variant report

Variant	rs6030018
Chromosome Location	chr20:40792096-40792097
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs1014757	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11907691	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11907769	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12625238	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13040788	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16986670	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1883376	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1883377	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2143632	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2223426	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2223718	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2867061	0.92[ASN][1000 genomes]
rs2867062	0.92[ASN][1000 genomes]
rs2867063	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2903465	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4375930	0.81[EUR][1000 genomes]
rs6016705	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6016706	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6016707	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6016708	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6016709	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6016710	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6016711	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6016712	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6016713	0.92[EUR][1000 genomes]
rs6016722	0.82[EUR][1000 genomes]
rs6030011	0.83[EUR][1000 genomes]
rs6030017	0.89[AFR][1000 genomes]
rs6030023	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6030026	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6030027	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6030029	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6030035	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6030036	0.92[EUR][1000 genomes]
rs6030037	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6030058	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6030061	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6030072	0.82[EUR][1000 genomes]
rs6030073	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6093584	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6093588	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6093589	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6093595	0.82[EUR][1000 genomes]
rs6093598	0.82[EUR][1000 genomes]
rs6102704	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6102713	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6102714	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6124427	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6124429	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6130062	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6130068	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6130071	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6130073	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6130074	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6130076	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6130081	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6513772	0.83[EUR][1000 genomes]
rs7270492	0.85[EUR][1000 genomes]
rs742290	0.83[AMR][1000 genomes];0.91[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	chr20:40790800-40795400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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