Variant report

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10957297	0.86[CEU][hapmap]
rs1149457	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1149470	0.91[EUR][1000 genomes]
rs1149471	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1149472	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1149473	0.91[EUR][1000 genomes]
rs1149474	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1149475	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1217098	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1217099	0.88[EUR][1000 genomes]
rs1217101	0.83[EUR][1000 genomes]
rs1217103	0.82[EUR][1000 genomes]
rs1217106	0.89[EUR][1000 genomes]
rs1217107	0.92[EUR][1000 genomes]
rs1217108	0.92[EUR][1000 genomes]
rs1217109	0.92[EUR][1000 genomes]
rs1217110	0.94[EUR][1000 genomes]
rs1238050	0.93[EUR][1000 genomes]
rs17215671	0.82[EUR][1000 genomes]
rs6472116	1.00[CHB][hapmap]
rs66503419	0.84[EUR][1000 genomes]
rs67801322	0.82[EUR][1000 genomes]
rs6992714	0.84[EUR][1000 genomes]
rs72649240	0.82[EUR][1000 genomes]
rs751769	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7824991	0.95[CEU][hapmap]
rs790563	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs790565	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs790566	0.87[EUR][1000 genomes]
rs790571	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs966294	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs978336	0.92[AMR][1000 genomes];0.93[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:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64540400-64545200	Weak transcription	Brain Germinal Matrix	brain
2	chr8:64540800-64544000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:64541800-64545400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr8:64543000-64545800	Enhancers	Fetal Brain Male	brain
5	chr8:64543400-64545400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr8:64543400-64546400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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