Variant report

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10484138	1.00[EUR][1000 genomes]
rs12587660	1.00[EUR][1000 genomes]
rs12590200	1.00[EUR][1000 genomes]
rs17117324	1.00[EUR][1000 genomes]
rs17117330	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17117384	1.00[EUR][1000 genomes]
rs17117392	1.00[EUR][1000 genomes]
rs17117436	1.00[EUR][1000 genomes]
rs35768970	1.00[EUR][1000 genomes]
rs60697834	1.00[EUR][1000 genomes]
rs7150950	1.00[EUR][1000 genomes]
rs7157030	1.00[EUR][1000 genomes]
rs73343607	1.00[EUR][1000 genomes]
rs73343612	1.00[EUR][1000 genomes]
rs73343613	1.00[EUR][1000 genomes]
rs73360736	1.00[EUR][1000 genomes]
rs73360750	1.00[EUR][1000 genomes]
rs73360772	1.00[EUR][1000 genomes]
rs73360774	1.00[EUR][1000 genomes]
rs73360778	1.00[EUR][1000 genomes]
rs73360779	1.00[EUR][1000 genomes]
rs74067029	1.00[EUR][1000 genomes]
rs74067184	1.00[EUR][1000 genomes]
rs74067185	1.00[EUR][1000 genomes]
rs74067200	1.00[EUR][1000 genomes]
rs74067202	1.00[EUR][1000 genomes]
rs74069203	1.00[EUR][1000 genomes]
rs74069241	1.00[EUR][1000 genomes]
rs74069243	1.00[EUR][1000 genomes]
rs74069244	1.00[EUR][1000 genomes]
rs74069245	1.00[EUR][1000 genomes]
rs74069248	1.00[EUR][1000 genomes]
rs74069249	1.00[EUR][1000 genomes]
rs74069251	1.00[EUR][1000 genomes]
rs8009617	1.00[EUR][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	nsv1054303	chr14:83018016-83258920	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv902124	chr14:83165520-83282163	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv902125	chr14:83196006-83245454	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:83233400-83251800	Weak transcription	Ovary	ovary

Quick Search: