Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1062229	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[MEX][hapmap];0.85[TSI][hapmap]
rs11626966	1.00[CHB][hapmap];1.00[MEX][hapmap]
rs11627899	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11628114	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17109491	1.00[CEU][hapmap]
rs17109498	1.00[CEU][hapmap]
rs17109521	1.00[CEU][hapmap]
rs17109529	0.84[CEU][hapmap]
rs17109538	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17109542	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17109558	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17109568	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17795976	1.00[ASN][1000 genomes]
rs17795982	1.00[ASN][1000 genomes]
rs1952501	1.00[CEU][hapmap]
rs2225270	1.00[CEU][hapmap]
rs55660351	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7153942	0.85[MEX][hapmap]
rs74037500	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74037501	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74039204	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8004569	1.00[CEU][hapmap];0.87[TSI][hapmap]
rs8004614	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][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	nsv901504	chr14:25184210-25646203	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv901509	chr14:25398571-25743484	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv901511	chr14:25505085-25588029	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs17109575	NYNRIN	cis	cerebellum	SCAN
rs17109575	DCAF11	cis	parietal	SCAN
rs17109575	APEX1	cis	parietal	SCAN
rs17109575	CEBPE	cis	parietal	SCAN

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25547000-25561600	Weak transcription	Pancreas	Pancrea
2	chr14:25551200-25555200	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr14:25551800-25555600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr14:25553200-25554000	Enhancers	Placenta Amnion	Placenta Amnion
5	chr14:25553200-25555200	Weak transcription	Primary monocytes fromperipheralblood	blood

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