Variant report

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs171457	0.84[TSI][hapmap]
rs1956014	1.00[LWK][hapmap]
rs1956016	0.92[CEU][hapmap];0.84[JPT][hapmap]
rs243146	0.84[CEU][hapmap]
rs243148	0.92[CEU][hapmap]
rs243149	0.84[CEU][hapmap]
rs243155	0.84[CEU][hapmap]
rs243156	0.84[CEU][hapmap]
rs243157	0.84[CEU][hapmap]
rs243159	0.84[CEU][hapmap]
rs243162	0.84[CEU][hapmap]
rs7155426	0.83[CEU][hapmap]
rs8021413	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap]

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	nsv902015	chr14:63261862-63356253	Enhancers Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1042953	chr14:63314591-63384260	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Major depressive disorder	23377640	GWAS catalog

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs8012941	SYT16	cis	cerebellum	SCAN

Chromatin state (count:0 , 50 per page) page:

No data

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