Variant report

Variant	rs6829716
Chromosome Location	chr4:48487814-48487815
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:48485954..48488857-chr4:48528912..48531083,2	K562	blood:

Extended variants
information (count: 92 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs10018344	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10029732	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10029785	0.86[JPT][hapmap]
rs10030853	0.86[EUR][1000 genomes]
rs10031777	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10049761	0.82[CEU][hapmap];0.86[CHB][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap]
rs10938534	0.87[CHB][hapmap];0.83[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.81[TSI][hapmap];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10938537	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs11734019	0.84[EUR][1000 genomes]
rs11737677	0.87[CHB][hapmap];0.83[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap]
rs11933919	0.86[EUR][1000 genomes]
rs11945562	0.87[CHB][hapmap];0.83[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12503599	0.87[EUR][1000 genomes]
rs12506098	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12645501	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12645951	0.86[JPT][hapmap]
rs13108474	0.84[EUR][1000 genomes]
rs13119041	0.87[CHB][hapmap];0.83[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap]
rs13127730	0.85[EUR][1000 genomes]
rs13138269	0.84[EUR][1000 genomes]
rs1472967	0.86[JPT][hapmap]
rs1507862	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1507865	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1702798	0.83[EUR][1000 genomes]
rs1712767	0.81[EUR][1000 genomes]
rs1712768	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1712772	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17575720	0.87[CHB][hapmap];0.95[JPT][hapmap];0.86[EUR][1000 genomes]
rs17656010	0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs17656040	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17656076	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17656094	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1876469	0.87[CHB][hapmap];0.83[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.80[EUR][1000 genomes]
rs2089503	0.86[EUR][1000 genomes]
rs2102397	0.87[CHB][hapmap];0.81[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap]
rs2291474	0.86[JPT][hapmap]
rs2291475	0.86[JPT][hapmap]
rs2354348	0.87[CHB][hapmap];0.83[CHD][hapmap];0.93[GIH][hapmap];0.91[JPT][hapmap];0.86[MKK][hapmap];0.85[EUR][1000 genomes]
rs28470767	0.87[CHB][hapmap];0.83[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.85[EUR][1000 genomes]
rs28733443	0.81[EUR][1000 genomes]
rs2940324	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2945330	0.92[EUR][1000 genomes]
rs3107022	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34558821	0.86[EUR][1000 genomes]
rs34635008	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs392187	0.86[JPT][hapmap]
rs404445	0.86[JPT][hapmap]
rs411261	0.86[JPT][hapmap]
rs421833	0.86[JPT][hapmap]
rs4536901	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.82[MKK][hapmap];0.91[TSI][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4695391	0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.92[MKK][hapmap];0.93[TSI][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59686413	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62311296	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6447640	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6447645	0.86[EUR][1000 genomes]
rs6447647	0.86[EUR][1000 genomes]
rs6811148	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6816010	0.86[JPT][hapmap]
rs6819159	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6821277	0.86[JPT][hapmap]
rs6829144	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6836632	0.86[ASW][hapmap];0.87[CHB][hapmap];0.83[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.82[MKK][hapmap];0.85[TSI][hapmap];0.94[YRI][hapmap];0.81[AFR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6838613	0.82[EUR][1000 genomes]
rs6843340	0.83[CHB][hapmap];0.83[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes]
rs6848073	0.91[JPT][hapmap]
rs6855022	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6856448	0.86[EUR][1000 genomes]
rs7438704	0.85[JPT][hapmap]
rs7654770	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7661515	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7667288	0.87[CHB][hapmap];0.83[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap]
rs7678379	0.87[CHB][hapmap];0.82[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7679210	0.87[CHB][hapmap];0.95[JPT][hapmap];0.86[EUR][1000 genomes]
rs7683398	0.87[CHB][hapmap];0.95[JPT][hapmap];0.87[EUR][1000 genomes]
rs7693461	0.87[CHB][hapmap];0.95[JPT][hapmap];0.86[EUR][1000 genomes]
rs7697851	0.87[CHB][hapmap];0.85[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs776584	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs776588	0.80[EUR][1000 genomes]
rs776590	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs776591	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs776601	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs796555	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.92[MKK][hapmap];0.93[TSI][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs937888	0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs937889	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs952289	0.87[CHB][hapmap];0.95[JPT][hapmap];0.86[EUR][1000 genomes]
rs9884546	0.84[EUR][1000 genomes]
rs992423	0.87[CHB][hapmap];0.83[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes];0.93[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	nsv470034	chr4:48427773-48605628	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
2	nsv594121	chr4:48427773-48605628	Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
3	nsv829925	chr4:48467693-48639342	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv879008	chr4:48473439-48496804	Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv879009	chr4:48476539-48494546	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs6829716	OCIAD2	cis	lymphoblastoid	seeQTL
rs6829716	OCIAD2	cis	cerebellum	SCAN
rs6829716	SLC10A4	cis	lung	GTEx

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48485000-48488800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr4:48485200-48490200	Active TSS	Cortex derived primary cultured neurospheres	brain
3	chr4:48486200-48492000	Weak transcription	Aorta	Aorta
4	chr4:48486600-48491800	Weak transcription	Pancreas	Pancrea
5	chr4:48487200-48505800	Weak transcription	A549	lung
6	chr4:48487400-48488200	Active TSS	K562	blood

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