Variant report

Variant	rs73003940
Chromosome Location	chr3:146295323-146295324
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:145940254..145941134-chr3:146295120..146295978,3	MCF-7	breast:
2	chr3:146051922..146052597-chr3:146295303..146296107,2	MCF-7	breast:
3	chr3:145936366..145937318-chr3:146295230..146296148,3	K562	blood:
4	chr3:145783012..145783944-chr3:146295169..146296067,2	K562	blood:
5	chr3:146044616..146045587-chr3:146295200..146296047,4	MCF-7	breast:
6	chr3:146051675..146052565-chr3:146295209..146295722,2	MCF-7	breast:

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10513291	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10513292	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10513293	0.94[ASN][1000 genomes]
rs10513294	0.94[ASN][1000 genomes]
rs10513295	0.94[ASN][1000 genomes]
rs10513296	0.94[ASN][1000 genomes]
rs12107033	0.94[ASN][1000 genomes]
rs12107454	0.94[ASN][1000 genomes]
rs12107668	0.94[ASN][1000 genomes]
rs12107910	0.92[ASN][1000 genomes]
rs12108037	0.94[ASN][1000 genomes]
rs1507360	0.93[ASN][1000 genomes]
rs16858574	0.90[ASN][1000 genomes]
rs16858584	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17354168	0.94[ASN][1000 genomes]
rs17354174	0.94[ASN][1000 genomes]
rs17354202	0.94[ASN][1000 genomes]
rs17367049	0.94[ASN][1000 genomes]
rs17367469	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17367802	0.94[ASN][1000 genomes]
rs17432180	0.94[ASN][1000 genomes]
rs17432313	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17432334	0.94[ASN][1000 genomes]
rs17432459	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17433008	0.94[ASN][1000 genomes]
rs17433127	0.92[ASN][1000 genomes]
rs17433365	0.94[ASN][1000 genomes]
rs17433421	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2008809	0.94[ASN][1000 genomes]
rs55706321	0.84[ASN][1000 genomes]
rs55775630	0.82[ASN][1000 genomes]
rs56303358	0.94[ASN][1000 genomes]
rs56763997	0.94[ASN][1000 genomes]
rs57144796	0.94[ASN][1000 genomes]
rs57564033	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58620235	0.94[ASN][1000 genomes]
rs60827860	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60897919	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61013048	0.94[ASN][1000 genomes]
rs61254159	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66460167	0.90[ASN][1000 genomes]
rs67360105	0.94[ASN][1000 genomes]
rs67479911	0.94[ASN][1000 genomes]
rs67678931	0.93[ASN][1000 genomes]
rs6784661	0.94[ASN][1000 genomes]
rs6787741	0.94[ASN][1000 genomes]
rs6787813	0.94[ASN][1000 genomes]
rs6795178	0.94[ASN][1000 genomes]
rs6797790	0.94[ASN][1000 genomes]
rs68009171	0.94[ASN][1000 genomes]
rs72988643	0.94[ASN][1000 genomes]
rs72988650	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72988655	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72988657	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72988660	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72988664	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72988675	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73003915	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73003942	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73003949	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73003950	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73003961	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73156949	0.93[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	nsv432489	chr3:146271370-146323969	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv877623	chr3:146278616-146319368	Enhancers Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv508253	chr3:146282620-146301477	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	1 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	chr3:146293800-146299800	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr3:146295200-146300000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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