Variant report

Variant	rs7016361
Chromosome Location	chr8:10867349-10867350
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 106 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:103)

rs_ID	r²[population]
rs10091913	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs10100449	1.00[CHB][hapmap]
rs10107384	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs10108304	1.00[CHB][hapmap]
rs10110123	1.00[CHB][hapmap]
rs10111751	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10216472	0.87[CEU][hapmap];0.93[EUR][1000 genomes]
rs10217059	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs10282848	1.00[CHB][hapmap]
rs11250103	0.91[CEU][hapmap];0.82[TSI][hapmap]
rs11250108	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11250110	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11250111	1.00[CHB][hapmap]
rs11250120	1.00[CHB][hapmap]
rs11779199	1.00[CEU][hapmap];0.86[GIH][hapmap];0.91[TSI][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11784312	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11785788	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11986748	1.00[CHB][hapmap]
rs11988372	1.00[CEU][hapmap];0.95[TSI][hapmap];0.97[EUR][1000 genomes]
rs11991121	1.00[CHB][hapmap]
rs11995682	0.97[EUR][1000 genomes]
rs11996027	1.00[CHB][hapmap]
rs11998417	1.00[CHB][hapmap]
rs12216757	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12216784	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12216875	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs17152862	1.00[CHB][hapmap]
rs17152881	1.00[CHB][hapmap]
rs17152921	1.00[CHB][hapmap]
rs17152930	1.00[CHB][hapmap]
rs17152938	1.00[CHB][hapmap]
rs17152978	1.00[CHB][hapmap]
rs17722940	1.00[CHB][hapmap]
rs17725809	1.00[CHB][hapmap]
rs17726352	1.00[CHB][hapmap]
rs17779093	1.00[CHB][hapmap]
rs2898254	1.00[CHB][hapmap]
rs2898258	1.00[CHB][hapmap]
rs35083028	0.89[ASN][1000 genomes]
rs4074356	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4074822	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4076425	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4270924	1.00[CHB][hapmap]
rs4320511	1.00[CEU][hapmap];0.87[GIH][hapmap];0.93[TSI][hapmap];0.94[EUR][1000 genomes]
rs4349949	1.00[CHB][hapmap]
rs4370496	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4386942	1.00[CHB][hapmap];0.89[ASN][1000 genomes]
rs4507728	1.00[CEU][hapmap];0.93[GIH][hapmap];0.88[TSI][hapmap];0.93[EUR][1000 genomes]
rs4840530	0.91[CEU][hapmap];0.82[TSI][hapmap]
rs4841469	0.82[EUR][1000 genomes]
rs4841471	1.00[CEU][hapmap];0.93[GIH][hapmap];0.93[TSI][hapmap];0.94[EUR][1000 genomes]
rs4841472	0.96[EUR][1000 genomes]
rs4841473	1.00[CHB][hapmap];0.80[AFR][1000 genomes]
rs4841474	0.94[EUR][1000 genomes]
rs4841475	0.97[EUR][1000 genomes]
rs4841476	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4841477	0.87[EUR][1000 genomes]
rs4841478	0.88[EUR][1000 genomes]
rs4841479	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56011306	0.89[ASN][1000 genomes]
rs56052312	0.89[EUR][1000 genomes]
rs56278516	0.83[EUR][1000 genomes]
rs56319439	0.83[EUR][1000 genomes]
rs61427182	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6601546	0.95[CEU][hapmap];0.93[EUR][1000 genomes]
rs6601550	1.00[CHB][hapmap]
rs67113145	0.89[ASN][1000 genomes]
rs6983680	1.00[CHB][hapmap]
rs6990395	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6994928	1.00[CHB][hapmap]
rs6999969	1.00[CHB][hapmap]
rs7000298	1.00[CHB][hapmap]
rs7000431	1.00[CHB][hapmap]
rs7001599	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7010099	1.00[CHB][hapmap]
rs7010126	1.00[CHB][hapmap]
rs7014291	1.00[CHB][hapmap]
rs73196884	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73196885	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73196888	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7350066	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7350072	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7350074	0.89[ASN][1000 genomes]
rs7813323	0.84[AFR][1000 genomes]
rs7820231	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7820777	1.00[CHB][hapmap]
rs7822400	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs7824797	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs7826561	0.94[EUR][1000 genomes]
rs7833832	0.97[EUR][1000 genomes]
rs7836687	0.94[EUR][1000 genomes]
rs7836720	1.00[CEU][hapmap];0.93[GIH][hapmap];0.91[TSI][hapmap];0.94[EUR][1000 genomes]
rs7837828	1.00[CEU][hapmap];0.95[GIH][hapmap];0.81[MEX][hapmap];0.91[TSI][hapmap];0.94[EUR][1000 genomes]
rs7838051	1.00[CHB][hapmap]
rs7838833	1.00[CEU][hapmap];0.89[GIH][hapmap];0.93[TSI][hapmap];0.96[EUR][1000 genomes]
rs7840980	1.00[CHB][hapmap]
rs7841435	1.00[CHB][hapmap]
rs7842214	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7845088	1.00[CHB][hapmap]
rs7846545	1.00[JPT][hapmap]
rs9329232	1.00[CEU][hapmap];0.93[GIH][hapmap];0.93[TSI][hapmap];0.95[EUR][1000 genomes]
rs9329237	1.00[CHB][hapmap]
rs9657542	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.96[EUR][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	nsv1035072	chr8:10819444-11480692	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv539473	chr8:10819444-11480692	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1022434	chr8:10866242-10916523	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs7016361	C8orf79	cis	cerebellum	SCAN
rs7016361	INPPL1	trans	cerebellum	SCAN
rs7016361	FLJ10661	cis	cerebellum	SCAN
rs7016361	C8orf5	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10859400-10872200	Weak transcription	Brain Angular Gyrus	brain
2	chr8:10865200-10870400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:10865400-10870400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr8:10865400-10870600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr8:10865800-10870600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr8:10866000-10870400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:10866400-10870600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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