Variant report

Variant	rs62109228
Chromosome Location	chr19:21536931-21536932
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 106 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs10414834	0.90[AMR][1000 genomes]
rs10420016	0.83[AFR][1000 genomes]
rs10424079	0.86[AMR][1000 genomes]
rs11666213	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs11666447	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11666525	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11666540	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11667103	0.91[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs11667361	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11667392	0.83[EUR][1000 genomes]
rs11669033	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11669790	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11670815	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11670868	0.95[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11672341	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11672583	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11673320	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11879901	0.88[EUR][1000 genomes]
rs13346641	0.86[AMR][1000 genomes]
rs1621154	0.87[EUR][1000 genomes]
rs1626404	0.87[EUR][1000 genomes]
rs1762578	0.87[EUR][1000 genomes]
rs17680605	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1781867	0.87[EUR][1000 genomes]
rs1781872	0.87[EUR][1000 genomes]
rs1879234	0.83[AFR][1000 genomes]
rs1967182	0.81[AMR][1000 genomes]
rs2061916	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2154302	0.86[EUR][1000 genomes]
rs2358993	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2359144	0.86[AMR][1000 genomes]
rs2359145	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2562405	0.86[AMR][1000 genomes]
rs2562408	0.83[AFR][1000 genomes]
rs2562411	0.86[AMR][1000 genomes]
rs2562413	0.83[AMR][1000 genomes]
rs2562416	0.90[AMR][1000 genomes]
rs2562466	0.83[AFR][1000 genomes]
rs2562468	0.83[AFR][1000 genomes]
rs2562471	0.83[AFR][1000 genomes]
rs2650776	0.90[AMR][1000 genomes]
rs2650825	0.83[AFR][1000 genomes]
rs2650844	0.86[AMR][1000 genomes]
rs2650848	0.86[AMR][1000 genomes]
rs2681377	0.83[AFR][1000 genomes]
rs2681389	0.83[AFR][1000 genomes]
rs2681392	0.83[AFR][1000 genomes]
rs279807	0.84[EUR][1000 genomes]
rs279809	0.85[EUR][1000 genomes]
rs3853837	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3853838	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4321312	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4327181	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4359573	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4544364	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4638726	0.86[AMR][1000 genomes]
rs55756795	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs55790393	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs55875743	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55899865	0.87[EUR][1000 genomes]
rs57299552	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs58412280	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs60173523	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61035285	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62107465	0.86[EUR][1000 genomes]
rs62107469	0.91[AFR][1000 genomes];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62107472	0.87[EUR][1000 genomes]
rs62107479	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62107531	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62107532	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62107534	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62107536	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62107539	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62107540	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62107541	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62109225	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62109226	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62109227	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62109229	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62110071	0.85[EUR][1000 genomes]
rs62110367	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62110377	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62110416	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62110420	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62110424	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62110426	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62110427	0.85[AMR][1000 genomes]
rs62110428	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs62110429	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7246339	0.91[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs7251135	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7258099	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7258473	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7258562	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73537884	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3518033	chr19:21278465-21747567	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3518034	chr19:21278465-21747567	ZNF genes & repeats Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	esv3414204	chr19:21301761-21839451	ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv911416	chr19:21388995-21548211	Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv911417	chr19:21388995-21564001	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	esv3325271	chr19:21445407-21792817	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
7	nsv911420	chr19:21454672-21613397	ZNF genes & repeats Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
8	esv2751783	chr19:21465822-21726337	Strong transcription ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
9	esv3363678	chr19:21483148-21756908	Strong transcription Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
10	nsv963023	chr19:21491992-21570395	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv578952	chr19:21535707-21868584	Genic enhancers Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs62109228	ZNF708	cis	Muscle Skeletal	GTEx
rs62109228	ZNF708	cis	lung	GTEx
rs62109228	RP11-678G14.2	cis	Whole Blood	GTEx
rs62109228	ZNF708	cis	Skin Sun Exposed Lower leg	GTEx
rs62109228	RP11-678G14.2	cis	Esophagus Muscularis	GTEx
rs62109228	RP11-678G14.3	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21535800-21537000	Weak transcription	Brain Substantia Nigra	brain
2	chr19:21536200-21541400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr19:21536200-21541400	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr19:21536800-21541200	Weak transcription	Dnd41	blood

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