Variant report

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10957297	0.86[CEU][hapmap]
rs1149456	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1149457	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1149470	0.92[EUR][1000 genomes]
rs1149471	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1149472	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1149473	0.92[EUR][1000 genomes]
rs1149474	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1149475	0.93[EUR][1000 genomes]
rs1217098	0.88[EUR][1000 genomes]
rs1217099	0.88[EUR][1000 genomes]
rs1217101	0.83[EUR][1000 genomes]
rs1217103	0.83[EUR][1000 genomes]
rs1217106	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1217107	0.93[EUR][1000 genomes]
rs1217108	0.93[EUR][1000 genomes]
rs1217109	0.93[EUR][1000 genomes]
rs1217110	0.95[EUR][1000 genomes]
rs1238050	0.94[EUR][1000 genomes]
rs17215671	0.83[EUR][1000 genomes]
rs6472116	1.00[CHB][hapmap]
rs66503419	0.84[EUR][1000 genomes]
rs67344323	0.81[EUR][1000 genomes]
rs67801322	0.83[EUR][1000 genomes]
rs6992714	0.84[EUR][1000 genomes]
rs72649240	0.83[EUR][1000 genomes]
rs751769	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7824991	0.95[CEU][hapmap]
rs790563	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs790564	0.80[EUR][1000 genomes]
rs790565	0.88[EUR][1000 genomes]
rs790566	0.88[EUR][1000 genomes]
rs966294	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs978336	0.80[AMR][1000 genomes];0.94[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	nsv831343	chr8:64436268-64642328	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr8:64554400-64558000	Weak transcription	Fetal Brain Female	brain
2	chr8:64556400-64558000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:64556400-64562000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:64557800-64559800	Enhancers	Fetal Brain Male	brain

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