Variant report

Variant	rs10412173
Chromosome Location	chr19:43054504-43054505
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10401178	0.90[AMR][1000 genomes]
rs10401428	0.85[AFR][1000 genomes]
rs10402853	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs10404589	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs10405037	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10405179	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs10406227	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs10408822	0.90[AMR][1000 genomes]
rs10412074	0.90[AMR][1000 genomes]
rs10412594	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs10414396	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs10415284	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10418090	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs10419543	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10420773	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs10423227	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs10423370	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10425199	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10425666	0.90[AMR][1000 genomes]
rs10426304	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11879033	0.86[AFR][1000 genomes]
rs11880554	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs11880876	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11882291	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs13346522	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs16975787	0.90[AMR][1000 genomes]
rs16975815	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs28403155	0.90[AMR][1000 genomes]
rs28433890	0.90[AMR][1000 genomes]
rs28473486	0.81[AFR][1000 genomes]
rs28588100	0.81[AFR][1000 genomes]
rs28602626	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs28635141	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs28660279	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41348545	0.90[AMR][1000 genomes]
rs41381546	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs41421250	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs57018456	0.90[AMR][1000 genomes]
rs58050143	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs58162305	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs58702905	0.84[AMR][1000 genomes]
rs60747186	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs61388144	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs6509015	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7247278	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7248907	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7249304	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7250501	0.90[AMR][1000 genomes]
rs7253634	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7256226	0.84[AFR][1000 genomes]
rs7256850	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs7259335	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs73558492	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73558498	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73560408	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs8101378	0.90[AMR][1000 genomes]
rs8105525	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs8106836	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs8107720	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs8108992	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs8110904	0.89[AMR][1000 genomes]
rs8110922	0.90[AMR][1000 genomes]
rs8111171	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs8111468	0.84[AMR][1000 genomes]
rs8112593	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8112915	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8113154	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8113448	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9749434	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs9916999	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526186	chr19:42676481-43203507	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
2	esv2422471	chr19:42733141-43669485	Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
3	esv2422468	chr19:42991289-43669027	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1057390	chr19:43003323-43173028	Enhancers Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv482597	chr19:43037214-43222644	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv2758501	chr19:43042747-43899053	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
7	esv2758763	chr19:43042747-43899053	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
8	nsv428023	chr19:43042747-43899053	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
9	esv3449805	chr19:43052508-43055085	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43050600-43067800	Weak transcription	Right Atrium	heart
2	chr19:43054000-43056800	Weak transcription	Adipose Nuclei	Adipose

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