Variant report

Variant	rs73026933
Chromosome Location	chr3:160922312-160922313
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:160918538..160922822-chr3:160936820..160940887,5	MCF-7	breast:
2	chr3:160922110..160927957-chr3:161089020..161092502,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000196542	Chromatin interaction
ENSG00000169251	Chromatin interaction

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs1017799	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12486069	0.90[ASN][1000 genomes]
rs12489004	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12489125	0.90[ASN][1000 genomes]
rs12490149	0.97[ASN][1000 genomes]
rs12494725	0.80[ASN][1000 genomes]
rs12496235	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs13315320	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs13319558	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs13319771	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs16831850	0.90[ASN][1000 genomes]
rs16831864	0.90[ASN][1000 genomes]
rs16831882	0.90[ASN][1000 genomes]
rs16831942	0.90[ASN][1000 genomes]
rs2306209	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs28451189	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs28704960	0.90[ASN][1000 genomes]
rs28713364	0.84[AMR][1000 genomes]
rs3925722	0.84[ASN][1000 genomes]
rs4296611	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4352387	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4468992	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4580574	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4635725	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs57903480	0.93[ASN][1000 genomes]
rs59567999	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59757775	0.93[ASN][1000 genomes]
rs59776766	0.90[ASN][1000 genomes]
rs60121330	0.90[ASN][1000 genomes]
rs6441350	0.90[ASN][1000 genomes]
rs6441363	0.81[AMR][1000 genomes]
rs6441365	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6441372	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6441375	0.90[ASN][1000 genomes]
rs6762064	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6774919	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6775446	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6775931	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6778186	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6782415	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6782518	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6785714	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6787447	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6788738	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6790805	0.97[ASN][1000 genomes]
rs6796168	0.90[ASN][1000 genomes]
rs6801664	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6805976	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73017340	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73026967	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73026968	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73026983	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73026987	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73026989	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73878309	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7615833	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7615868	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7624791	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7626773	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7634299	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7651924	0.90[ASN][1000 genomes]
rs7652624	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9290070	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9290071	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9810351	0.90[ASN][1000 genomes]
rs9812574	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9818470	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9818835	0.90[ASN][1000 genomes]
rs9818992	0.85[ASN][1000 genomes]
rs9819793	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9822705	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9822916	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9823424	0.90[ASN][1000 genomes]
rs9824535	0.90[ASN][1000 genomes]
rs9824805	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9826857	0.90[ASN][1000 genomes]
rs9830183	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9833270	1.00[ASN][1000 genomes]
rs9834806	0.81[AMR][1000 genomes]
rs9835530	0.90[ASN][1000 genomes]
rs9838945	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9841871	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9842290	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9847842	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9851699	0.90[ASN][1000 genomes]
rs9855112	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9855572	0.90[ASN][1000 genomes]
rs9856742	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9858907	0.90[ASN][1000 genomes]
rs9859641	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9860980	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9862867	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9871753	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9876077	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9877309	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9880536	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9884100	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9985364	0.86[AMR][1000 genomes];1.00[ASN][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	nsv931072	chr3:160669567-161159779	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv1015063	chr3:160918307-161024070	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 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	chr3:160915000-160927000	Weak transcription	Aorta	Aorta

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