Variant report

Variant	rs12664634
Chromosome Location	chr6:86579414-86579415
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 20 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1059307	0.82[CHB][hapmap];0.90[CHD][hapmap]
rs10944137	0.90[CEU][hapmap]
rs1173418	0.82[CHB][hapmap]
rs11752180	0.81[ASN][1000 genomes]
rs11752223	0.81[ASN][1000 genomes]
rs11755642	0.90[CEU][hapmap]
rs11758508	0.90[CEU][hapmap]
rs12055653	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12190603	0.94[CEU][hapmap]
rs12192546	0.90[CEU][hapmap]
rs12193904	0.90[CEU][hapmap]
rs12202712	0.82[ASN][1000 genomes]
rs12209668	0.80[ASN][1000 genomes]
rs12212480	0.90[CEU][hapmap]
rs12216103	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12660846	0.81[ASN][1000 genomes]
rs12661231	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12661611	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12665464	0.90[CEU][hapmap];0.81[ASN][1000 genomes]
rs13207173	0.90[CEU][hapmap]
rs13212415	0.85[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs1335442	0.90[CEU][hapmap]
rs1447159	0.85[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs1470531	0.90[CEU][hapmap];0.83[CHB][hapmap]
rs1838954	0.80[ASN][1000 genomes]
rs1838955	0.80[ASN][1000 genomes]
rs1838956	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1838957	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1838958	0.80[ASN][1000 genomes]
rs1838959	0.80[ASN][1000 genomes]
rs1995688	0.81[CEU][hapmap]
rs2084293	0.80[ASN][1000 genomes]
rs2084294	0.80[ASN][1000 genomes]
rs2121594	0.90[CEU][hapmap]
rs2121595	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2225754	0.90[CEU][hapmap]
rs3087978	0.82[CHB][hapmap]
rs36035797	0.80[ASN][1000 genomes]
rs4706252	0.80[ASN][1000 genomes]
rs4706253	0.80[ASN][1000 genomes]
rs4707235	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6454487	0.90[CEU][hapmap];0.80[CHD][hapmap];0.83[MEX][hapmap]
rs6454492	0.85[ASN][1000 genomes]
rs6454504	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6929514	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7739241	0.90[CEU][hapmap];0.83[CHB][hapmap];0.89[MEX][hapmap];0.82[ASN][1000 genomes]
rs7755730	0.80[ASN][1000 genomes]
rs7755790	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7770835	0.84[ASN][1000 genomes]
rs9647601	0.90[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028293	chr6:86353958-86778912	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	100 gene(s)	inside rSNPs	diseases
2	nsv538350	chr6:86353958-86778912	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	100 gene(s)	inside rSNPs	diseases
3	nsv886335	chr6:86445651-86669361	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1022618	chr6:86465365-87432069	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv538352	chr6:86465365-87432069	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv1033637	chr6:86482045-86701733	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv538353	chr6:86482045-86701733	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	esv1802672	chr6:86546123-86662267	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1018453	chr6:86555984-86761120	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv463940	chr6:86576854-86648436	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv604095	chr6:86576854-86648436	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv604096	chr6:86576854-86649705	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:20)

SNP	Gene	Cis/trans	Tissue	Source
rs12664634	C6orf160	cis	normal skin	skin_eQTL
rs12664634	SNHG5	cis	Artery Aorta	GTEx
rs12664634	SNHG5	cis	Nerve Tibial	GTEx
rs12664634	C6orf160	cis	uninvolved skin	skin_eQTL
rs12664634	SNHG5	cis	lung	GTEx
rs12664634	SNHG5	cis	Skin Sun Exposed Lower leg	GTEx
rs12664634	SNHG5	cis	Adipose Subcutaneous	GTEx
rs12664634	SNHG5	cis	Artery Tibial	GTEx
rs12664634	SNHG5	cis	Esophagus Mucosa	GTEx
rs12664634	SNHG5	cis	Whole Blood	GTEx
rs12664634	SNHG5	cis	multi-tissue	Pritchard
rs12664634	SNHG5	cis	Muscle Skeletal	GTEx
rs12664634	SNHG5	cis	Stomach	GTEx
rs12664634	SNHG5	cis	Thyroid	GTEx
rs12664634	NT5E	cis	Thyroid	GTEx
rs12664634	C6orf160	cis	lesional skin	skin_eQTL
rs12664634	SNHG5	cis	Esophagus Muscularis	GTEx
rs12664634	SNHG5	Cis_1M	lymphoblastoid	RTeQTL
rs12664634	SNHG5	cis	lymphoblastoid	seeQTL
rs12664634	SNHG5	cis	Heart Left Ventricle	GTEx

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:86575200-86583400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:86576800-86580000	Weak transcription	Psoas Muscle	Psoas
3	chr6:86579200-86584000	Weak transcription	Ovary	ovary

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