Variant report

Variant	rs17691911
Chromosome Location	chr3:179632808-179632809
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	chr3:179627375..179629494-chr3:179631939..179634433,2	MCF-7	breast:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11708154	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11709733	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11718907	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1404271	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1599791	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16830940	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17748709	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17748864	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2302741	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2302742	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28619517	0.92[EUR][1000 genomes]
rs41265425	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4146789	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56263652	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56395499	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56677569	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56836862	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs57376419	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs57823511	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59018122	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59453720	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73058681	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73060731	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73060760	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73060761	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7630877	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7637613	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7646149	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9290685	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs940523	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9682757	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9831383	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9836757	0.94[AMR][1000 genomes];0.95[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	nsv829807	chr3:179527567-179745153	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv829808	chr3:179574614-179754321	Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179624800-179639000	Weak transcription	Brain Substantia Nigra	brain
2	chr3:179630000-179638800	Weak transcription	Brain Angular Gyrus	brain
3	chr3:179631800-179633000	Enhancers	Brain Hippocampus Middle	brain
4	chr3:179632000-179634200	Strong transcription	Dnd41	blood

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