Variant report

Variant	rs13279328
Chromosome Location	chr8:130066249-130066250
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10105449	0.91[EUR][1000 genomes]
rs10435553	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10435554	0.80[EUR][1000 genomes]
rs10435555	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10448000	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10464829	0.93[ASW][hapmap];0.93[YRI][hapmap]
rs10808576	0.85[AFR][1000 genomes]
rs1157275	0.86[EUR][1000 genomes]
rs12541644	0.80[EUR][1000 genomes]
rs12541935	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12543251	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1372442	0.86[EUR][1000 genomes]
rs1372443	0.86[EUR][1000 genomes]
rs1372453	0.89[EUR][1000 genomes]
rs34294444	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34294531	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34495693	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34871599	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs34892339	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35658327	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35721910	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4236737	0.86[EUR][1000 genomes]
rs4266613	0.86[AFR][1000 genomes]
rs4302810	0.86[EUR][1000 genomes]
rs4326354	0.85[AFR][1000 genomes]
rs4333552	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4371972	0.86[EUR][1000 genomes]
rs4493878	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4526322	0.82[EUR][1000 genomes]
rs4566994	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4613963	0.93[EUR][1000 genomes]
rs4636163	0.93[EUR][1000 genomes]
rs4644199	0.85[EUR][1000 genomes]
rs56198698	0.84[AFR][1000 genomes]
rs57797099	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59669561	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6470676	0.86[EUR][1000 genomes]
rs6470677	0.86[EUR][1000 genomes]
rs6470692	0.93[EUR][1000 genomes]
rs6470694	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs66879839	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs67401439	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67459926	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6989490	0.80[EUR][1000 genomes]
rs7004935	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7015312	0.82[AFR][1000 genomes]
rs73382040	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73382043	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7815639	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7816364	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7820114	0.85[EUR][1000 genomes]
rs7832166	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7832400	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7832457	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7832834	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7833157	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7834731	0.91[EUR][1000 genomes]
rs7836429	0.85[EUR][1000 genomes]
rs7837430	0.85[AFR][1000 genomes]
rs7840107	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7843664	0.90[EUR][1000 genomes]
rs9643242	0.80[EUR][1000 genomes]
rs9650100	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9650101	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[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	nsv891442	chr8:130016499-130130604	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv891443	chr8:130016499-130220746	Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv891444	chr8:130024642-130130604	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130061000-130071000	Weak transcription	Thymus	Thymus
2	chr8:130062200-130071000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:130062400-130071200	Weak transcription	Fetal Thymus	thymus
4	chr8:130064400-130066400	Genic enhancers	Dnd41	blood
5	chr8:130065400-130066400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr8:130065400-130068600	Enhancers	K562	blood
7	chr8:130066200-130066400	Enhancers	Pancreas	Pancrea

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