Variant report

Variant	rs73182103
Chromosome Location	chr3:94721251-94721252
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:94715493..94717175-chr3:94721008..94723203,2	MCF-7	breast:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11915767	0.92[EUR][1000 genomes]
rs11919547	0.96[EUR][1000 genomes]
rs11925508	0.96[EUR][1000 genomes]
rs11927923	0.81[EUR][1000 genomes]
rs1432470	0.90[EUR][1000 genomes]
rs16853213	0.81[EUR][1000 genomes]
rs1897462	0.90[EUR][1000 genomes]
rs28589479	0.86[EUR][1000 genomes]
rs300077	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs441713	0.86[EUR][1000 genomes]
rs61005216	0.92[EUR][1000 genomes]
rs61562444	0.92[EUR][1000 genomes]
rs6804802	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73178274	0.98[EUR][1000 genomes]
rs73178277	0.98[EUR][1000 genomes]
rs73178279	0.98[EUR][1000 genomes]
rs73178292	0.92[EUR][1000 genomes]
rs73179414	0.83[EUR][1000 genomes]
rs73179420	0.91[EUR][1000 genomes]
rs73179422	0.90[EUR][1000 genomes]
rs73179424	0.91[EUR][1000 genomes]
rs73179452	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73179462	0.91[EUR][1000 genomes]
rs73179464	0.91[EUR][1000 genomes]
rs73179469	0.92[EUR][1000 genomes]
rs73179470	0.92[EUR][1000 genomes]
rs73179478	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73179483	0.96[EUR][1000 genomes]
rs73179490	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73179494	0.96[EUR][1000 genomes]
rs73179499	0.96[EUR][1000 genomes]
rs73180219	0.92[EUR][1000 genomes]
rs73181203	0.90[EUR][1000 genomes]
rs73181208	0.98[EUR][1000 genomes]
rs73181209	0.98[EUR][1000 genomes]
rs73847061	0.91[EUR][1000 genomes]
rs7613024	0.86[EUR][1000 genomes]
rs7619245	0.83[EUR][1000 genomes]
rs7625489	0.98[EUR][1000 genomes]
rs7625700	0.92[EUR][1000 genomes]
rs7631481	0.86[EUR][1000 genomes]
rs7635954	0.91[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877169	chr3:94675697-94840854	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 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	chr3:94720400-94722600	Enhancers	Pancreatic Islets	Pancreatic Islet

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