Variant report

Variant	rs906994
Chromosome Location	chr8:78544857-78544858
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10087157	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10090012	0.99[ASN][1000 genomes]
rs10090643	1.00[ASN][1000 genomes]
rs10103850	0.99[ASN][1000 genomes]
rs10103975	0.99[ASN][1000 genomes]
rs10105170	0.99[ASN][1000 genomes]
rs10111403	0.98[ASN][1000 genomes]
rs1039856	0.99[ASN][1000 genomes]
rs1039857	0.99[ASN][1000 genomes]
rs1039858	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11986712	1.00[ASN][1000 genomes]
rs12334946	0.99[ASN][1000 genomes]
rs12334948	0.99[ASN][1000 genomes]
rs12676452	1.00[ASN][1000 genomes]
rs12680616	1.00[ASN][1000 genomes]
rs1397103	0.99[ASN][1000 genomes]
rs1510116	1.00[ASN][1000 genomes]
rs1510117	1.00[ASN][1000 genomes]
rs1510122	0.99[ASN][1000 genomes]
rs1510123	0.99[ASN][1000 genomes]
rs1510124	0.99[ASN][1000 genomes]
rs1519361	0.86[ASN][1000 genomes]
rs1567426	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1567427	1.00[ASN][1000 genomes]
rs1567428	1.00[ASN][1000 genomes]
rs17382111	1.00[ASN][1000 genomes]
rs17382125	1.00[ASN][1000 genomes]
rs17382153	1.00[ASN][1000 genomes]
rs17382466	1.00[ASN][1000 genomes]
rs17383009	0.99[ASN][1000 genomes]
rs17466971	1.00[ASN][1000 genomes]
rs17467349	0.99[ASN][1000 genomes]
rs2063336	0.99[ASN][1000 genomes]
rs2063337	0.99[ASN][1000 genomes]
rs2136642	0.99[ASN][1000 genomes]
rs2175233	0.99[ASN][1000 genomes]
rs2221742	0.99[ASN][1000 genomes]
rs2339071	0.99[ASN][1000 genomes]
rs34860047	1.00[ASN][1000 genomes]
rs365235	0.88[EUR][1000 genomes]
rs366101	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs367237	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs380777	0.88[EUR][1000 genomes]
rs3920192	1.00[ASN][1000 genomes]
rs416406	0.88[EUR][1000 genomes]
rs424090	0.88[EUR][1000 genomes]
rs428631	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs437478	0.83[EUR][1000 genomes]
rs441257	0.88[EUR][1000 genomes]
rs444044	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs475495	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6998256	0.99[ASN][1000 genomes]
rs6998776	0.99[ASN][1000 genomes]
rs7003266	0.99[ASN][1000 genomes]
rs7006306	0.99[ASN][1000 genomes]
rs7016106	1.00[ASN][1000 genomes]
rs7016172	0.96[ASN][1000 genomes]
rs7016476	0.99[ASN][1000 genomes]
rs906995	1.00[ASN][1000 genomes]
rs906996	1.00[ASN][1000 genomes]
rs9298303	0.91[ASN][1000 genomes]
rs9298304	0.90[ASN][1000 genomes]
rs9785092	0.99[ASN][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	nsv891049	chr8:78325885-78565529	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1033669	chr8:78414508-78704839	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1016506	chr8:78414508-78750343	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv539650	chr8:78414508-78750343	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv465720	chr8:78452222-78551702	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv611568	chr8:78452222-78551702	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv1033074	chr8:78489781-78614082	Active TSS Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	esv2752462	chr8:78492584-78669157	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv1027584	chr8:78539823-78806136	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv1021008	chr8:78540652-78902770	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv539651	chr8:78540652-78902770	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:78541600-78547000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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