Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10220095	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10507554	0.80[ASN][1000 genomes]
rs13378547	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1413072	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1413073	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1413074	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1413075	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17069824	0.83[ASN][1000 genomes]
rs2065563	1.00[ASN][1000 genomes]
rs6561365	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6561366	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7320763	1.00[ASN][1000 genomes]
rs7330865	1.00[ASN][1000 genomes]
rs8000212	1.00[ASN][1000 genomes]
rs8001433	1.00[ASN][1000 genomes]
rs9316288	0.97[ASN][1000 genomes]
rs9316289	0.97[ASN][1000 genomes]
rs9316290	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9591026	1.00[ASN][1000 genomes]
rs9591027	0.97[ASN][1000 genomes]
rs9591028	1.00[ASN][1000 genomes]
rs9591029	1.00[ASN][1000 genomes]
rs9591032	0.80[ASN][1000 genomes]
rs9595636	0.83[ASN][1000 genomes]
rs9595638	0.83[ASN][1000 genomes]
rs9595643	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	esv2763019	chr13:47348229-48123447	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv3394678	chr13:47678184-48039379	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv832599	chr13:47703075-47873855	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12016712	C12orf32	trans	cerebellum	SCAN

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:47862800-47874200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr13:47863200-47865400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr13:47864200-47865800	Enhancers	Hela-S3	cervix
4	chr13:47865200-47865600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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