Variant report

Variant	rs6108950
Chromosome Location	chr20:11365154-11365155
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:11330194..11333067-chr20:11363546..11365974,2	MCF-7	breast:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10432740	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11087024	0.82[AFR][1000 genomes]
rs2207125	0.88[AFR][1000 genomes]
rs2207127	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2207128	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2327372	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2327373	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2327374	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2327375	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2327376	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2327400	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2876223	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35455280	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4522681	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6033101	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6033103	0.80[EUR][1000 genomes]
rs6033104	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6033109	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6040526	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6040529	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6040530	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6040531	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6040533	0.90[EUR][1000 genomes]
rs6074280	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6074286	0.80[EUR][1000 genomes]
rs6074296	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6078128	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6078129	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6078153	0.81[EUR][1000 genomes]
rs6078154	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6078155	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6078156	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6078158	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6078160	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6104744	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6104746	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6108946	0.81[EUR][1000 genomes]
rs6108947	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6108949	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6134231	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6134235	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7269125	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs764354	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs764355	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8119692	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065969	chr20:10850562-11464172	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv544181	chr20:10850562-11464172	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv585415	chr20:11134907-11383327	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 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	chr20:11363400-11367600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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