Variant report

Variant	rs930050
Chromosome Location	chr5:91103192-91103193
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1366129	0.98[ASN][1000 genomes]
rs1863948	0.95[ASN][1000 genomes]
rs1863949	0.98[ASN][1000 genomes]
rs1863950	0.98[ASN][1000 genomes]
rs2367826	0.99[ASN][1000 genomes]
rs2367828	0.99[ASN][1000 genomes]
rs2367829	0.99[ASN][1000 genomes]
rs2860382	0.98[ASN][1000 genomes]
rs2887093	0.99[ASN][1000 genomes]
rs2887094	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913415	0.99[ASN][1000 genomes]
rs2913416	0.98[ASN][1000 genomes]
rs2913417	0.99[ASN][1000 genomes]
rs2913418	0.99[ASN][1000 genomes]
rs2913419	0.99[ASN][1000 genomes]
rs2913420	0.99[ASN][1000 genomes]
rs2913421	0.99[ASN][1000 genomes]
rs2913440	0.99[ASN][1000 genomes]
rs2913442	0.99[ASN][1000 genomes]
rs2913443	0.99[ASN][1000 genomes]
rs2913444	0.80[ASN][1000 genomes]
rs2913447	0.98[ASN][1000 genomes]
rs2913448	0.98[ASN][1000 genomes]
rs2913449	0.98[ASN][1000 genomes]
rs2913450	0.98[ASN][1000 genomes]
rs2913451	0.98[ASN][1000 genomes]
rs2913452	0.96[ASN][1000 genomes]
rs2973853	0.99[ASN][1000 genomes]
rs2973854	0.98[ASN][1000 genomes]
rs2973855	0.96[ASN][1000 genomes]
rs2973856	0.99[ASN][1000 genomes]
rs2973863	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2973864	0.98[ASN][1000 genomes]
rs2973865	0.98[ASN][1000 genomes]
rs2973866	0.96[ASN][1000 genomes]
rs2973867	0.96[ASN][1000 genomes]
rs4270726	0.95[ASN][1000 genomes]
rs4397159	0.95[ASN][1000 genomes]
rs4398667	0.95[ASN][1000 genomes]
rs6865934	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9293576	0.95[ASN][1000 genomes]
rs9293577	0.95[ASN][1000 genomes]
rs930051	0.99[ASN][1000 genomes]

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	nsv830394	chr5:90944049-91107749	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv830395	chr5:90955521-91135272	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv882370	chr5:90986181-91287437	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv882372	chr5:91018052-91221647	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1017504	chr5:91092920-91178854	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs930050	C5orf36	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91099200-91104000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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