Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10088688	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs10103830	0.82[CHB][hapmap]
rs1011587	0.81[JPT][hapmap]
rs11778422	0.86[ASN][1000 genomes]
rs13264559	0.81[JPT][hapmap]
rs17071958	0.82[CHB][hapmap]
rs17071968	0.82[CHB][hapmap]
rs2924719	0.86[CHB][hapmap]
rs2924720	0.86[CHB][hapmap];0.84[CHD][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs2924721	0.82[ASN][1000 genomes]
rs2924723	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs2924726	1.00[CEU][hapmap];0.90[TSI][hapmap];0.82[EUR][1000 genomes]
rs2977732	0.82[JPT][hapmap]
rs2977733	0.82[CHB][hapmap]
rs4329292	0.82[JPT][hapmap]
rs4495447	0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs4517143	0.81[CHD][hapmap]
rs4593564	0.82[CHB][hapmap]
rs4614018	0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs4875427	0.86[CHB][hapmap];0.86[CHD][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs6558951	0.82[JPT][hapmap]
rs9657374	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.97[TSI][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9657406	0.82[CHB][hapmap]
rs9657407	0.82[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv609876	chr8:4494811-5092970	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1029480	chr8:4497596-5081032	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv498130	chr8:4532988-5176376	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1031026	chr8:4771072-5054326	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1031402	chr8:4827087-4842934	Strong transcription Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4831400-4838800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:4832000-4848200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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