Variant report

Variant	rs6916639
Chromosome Location	chr6:109858772-109858773
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 88 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10434873	0.80[ASN][1000 genomes]
rs10457201	0.82[ASN][1000 genomes]
rs10872041	0.85[ASN][1000 genomes]
rs10872047	0.82[ASN][1000 genomes]
rs1115977	0.82[ASN][1000 genomes]
rs11966009	0.80[ASN][1000 genomes]
rs12524352	0.82[ASN][1000 genomes]
rs1303981	0.80[ASN][1000 genomes]
rs1321327	0.80[ASN][1000 genomes]
rs1358759	0.85[ASN][1000 genomes]
rs1474959	0.82[ASN][1000 genomes]
rs1570011	0.82[ASN][1000 genomes]
rs1570012	0.82[ASN][1000 genomes]
rs1570013	0.80[ASN][1000 genomes]
rs1590187	0.85[ASN][1000 genomes]
rs17070656	0.80[ASN][1000 genomes]
rs1967725	0.82[ASN][1000 genomes]
rs1969710	0.80[ASN][1000 genomes]
rs1985123	0.85[ASN][1000 genomes]
rs1998812	0.85[ASN][1000 genomes]
rs2064820	0.85[ASN][1000 genomes]
rs2357123	0.85[ASN][1000 genomes]
rs2357125	0.82[ASN][1000 genomes]
rs4523125	0.82[ASN][1000 genomes]
rs4946986	0.85[ASN][1000 genomes]
rs4946987	0.81[ASN][1000 genomes]
rs4946989	0.82[ASN][1000 genomes]
rs4946991	0.81[ASN][1000 genomes]
rs4946992	0.82[ASN][1000 genomes]
rs60640103	0.80[ASN][1000 genomes]
rs6568580	0.85[ASN][1000 genomes]
rs6916239	0.84[ASN][1000 genomes]
rs6929823	0.82[ASN][1000 genomes]
rs7453835	0.82[ASN][1000 genomes]
rs7454678	0.81[ASN][1000 genomes]
rs7749386	0.82[ASN][1000 genomes]
rs7754118	0.82[ASN][1000 genomes]
rs7754606	0.82[ASN][1000 genomes]
rs9320289	0.80[ASN][1000 genomes]
rs9320292	0.80[ASN][1000 genomes]
rs9320294	0.86[ASN][1000 genomes]
rs9320295	0.86[ASN][1000 genomes]
rs9320296	0.86[ASN][1000 genomes]
rs9320299	0.82[ASN][1000 genomes]
rs9320304	0.82[ASN][1000 genomes]
rs9320305	0.82[ASN][1000 genomes]
rs9372216	0.82[ASN][1000 genomes]
rs9374092	0.85[ASN][1000 genomes]
rs9374095	0.85[ASN][1000 genomes]
rs9374097	0.85[ASN][1000 genomes]
rs9374099	0.85[ASN][1000 genomes]
rs9374108	0.82[ASN][1000 genomes]
rs9384713	0.85[ASN][1000 genomes]
rs9384715	0.82[ASN][1000 genomes]
rs9384716	0.82[ASN][1000 genomes]
rs9386810	0.80[ASN][1000 genomes]
rs9386812	0.85[ASN][1000 genomes]
rs9386813	0.85[ASN][1000 genomes]
rs9386816	0.80[ASN][1000 genomes]
rs9386818	0.82[ASN][1000 genomes]
rs9386823	0.82[ASN][1000 genomes]
rs9386824	0.82[ASN][1000 genomes]
rs9386825	0.82[ASN][1000 genomes]
rs9398204	0.86[ASN][1000 genomes]
rs9398205	0.80[ASN][1000 genomes]
rs9398206	0.82[ASN][1000 genomes]
rs9400291	0.85[ASN][1000 genomes]
rs9400294	0.85[ASN][1000 genomes]
rs9400295	0.85[ASN][1000 genomes]
rs9400301	0.82[ASN][1000 genomes]
rs942923	0.85[ASN][1000 genomes]
rs942924	0.85[ASN][1000 genomes]
rs9480969	0.80[ASN][1000 genomes]
rs9480973	0.85[ASN][1000 genomes]
rs9480974	0.85[ASN][1000 genomes]
rs9480976	0.85[ASN][1000 genomes]
rs9480982	0.81[ASN][1000 genomes]
rs9487141	0.85[ASN][1000 genomes]
rs9487148	0.81[ASN][1000 genomes]
rs9487156	0.82[ASN][1000 genomes]
rs9487160	0.80[ASN][1000 genomes]
rs9487164	0.81[ASN][1000 genomes]
rs9487170	0.82[ASN][1000 genomes]
rs9487171	0.81[ASN][1000 genomes]
rs9487172	0.80[ASN][1000 genomes]
rs9986507	0.82[ASN][1000 genomes]

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	nsv1026012	chr6:109851638-109999379	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv604484	chr6:109851937-109997529	ZNF genes & repeats Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6916639	C6orf199	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109838600-109861400	Weak transcription	Thymus	Thymus
2	chr6:109848400-109865600	Weak transcription	Aorta	Aorta
3	chr6:109848400-109870400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr6:109850800-109870000	Weak transcription	Left Ventricle	heart
5	chr6:109852200-109878400	Weak transcription	Pancreas	Pancrea

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