Variant report

Variant	rs4865846
Chromosome Location	chr5:49867597-49867598
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 101 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10038842	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10039639	0.91[CEU][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10041633	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10043477	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10045122	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10052001	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10070517	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10071272	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10434558	1.00[CEU][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10471888	1.00[ASN][1000 genomes]
rs10471893	1.00[ASN][1000 genomes]
rs10471940	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10471956	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10755235	0.90[CEU][hapmap]
rs10940423	0.82[EUR][1000 genomes]
rs10940424	0.87[EUR][1000 genomes]
rs10940497	1.00[CEU][hapmap]
rs11738761	0.87[EUR][1000 genomes]
rs11741205	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11745945	0.87[EUR][1000 genomes]
rs11750771	1.00[CEU][hapmap]
rs12188262	1.00[CEU][hapmap]
rs12188654	1.00[CEU][hapmap]
rs12518710	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12653803	0.81[EUR][1000 genomes]
rs13159764	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13162921	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13164951	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs13355372	1.00[ASN][1000 genomes]
rs13355434	1.00[ASN][1000 genomes]
rs1375127	1.00[CEU][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs154138	1.00[CEU][hapmap]
rs16884018	1.00[CEU][hapmap]
rs169497	0.91[CEU][hapmap]
rs182230	1.00[CEU][hapmap]
rs1839128	0.91[CEU][hapmap];0.87[EUR][1000 genomes]
rs1900738	0.83[EUR][1000 genomes]
rs1972980	0.85[EUR][1000 genomes]
rs1988613	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2034392	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2034393	0.87[EUR][1000 genomes]
rs2034394	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2121979	0.87[EUR][1000 genomes]
rs2166893	0.87[EUR][1000 genomes]
rs2166894	0.87[EUR][1000 genomes]
rs2548581	1.00[CEU][hapmap]
rs2548582	0.81[CEU][hapmap]
rs2697662	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs282549	1.00[ASN][1000 genomes]
rs282550	1.00[CEU][hapmap]
rs282552	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs282553	1.00[CEU][hapmap]
rs282559	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs282561	1.00[CEU][hapmap]
rs4029420	1.00[CEU][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4101529	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4282859	0.87[EUR][1000 genomes]
rs4415044	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4440312	0.85[EUR][1000 genomes]
rs4865628	1.00[CEU][hapmap]
rs4865895	0.87[EUR][1000 genomes]
rs4865896	0.84[EUR][1000 genomes]
rs4865974	1.00[JPT][hapmap]
rs4866001	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6450292	0.85[EUR][1000 genomes]
rs6450359	1.00[CEU][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6863575	0.84[EUR][1000 genomes]
rs6869356	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6872070	0.87[EUR][1000 genomes]
rs6872496	1.00[CEU][hapmap]
rs6879306	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6886872	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6888147	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6890519	1.00[CEU][hapmap]
rs6890869	1.00[CEU][hapmap]
rs73093361	1.00[ASN][1000 genomes]
rs73112331	1.00[ASN][1000 genomes]
rs73112340	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7449019	1.00[ASN][1000 genomes]
rs7709831	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7710150	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7711839	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7721050	0.85[EUR][1000 genomes]
rs7723361	0.83[CEU][hapmap];1.00[JPT][hapmap]
rs7728222	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7730847	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7734389	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs895801	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs921210	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv1032003	chr5:49455624-49881491	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1016583	chr5:49455624-50116720	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1023140	chr5:49455624-50121623	Enhancers Active TSS Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1023981	chr5:49584188-49871537	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv537757	chr5:49584188-49871537	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1022067	chr5:49584188-49960083	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv537758	chr5:49584188-49960083	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv918220	chr5:49584188-50111282	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv931010	chr5:49584189-50118254	Genic enhancers Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv523212	chr5:49597497-50058043	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	esv2757995	chr5:49748352-50058182	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	esv2759342	chr5:49748352-50058182	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4865846	PARP8	Cis_1M	lymphoblastoid	RTeQTL
rs4865846	LOC647121	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:49861000-49870000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr5:49862600-49870000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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