Variant report

Variant	rs6990512
Chromosome Location	chr8:34770105-34770106
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10086581	1.00[EUR][1000 genomes]
rs10087159	1.00[EUR][1000 genomes]
rs10090951	1.00[EUR][1000 genomes]
rs10092592	0.98[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10096301	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10096449	0.91[EUR][1000 genomes]
rs10101460	1.00[EUR][1000 genomes]
rs10102567	1.00[EUR][1000 genomes]
rs10107819	0.98[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10111345	1.00[EUR][1000 genomes]
rs11985581	0.98[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11990228	0.90[EUR][1000 genomes]
rs16883225	0.90[EUR][1000 genomes]
rs16883229	0.90[EUR][1000 genomes]
rs17249093	0.90[EUR][1000 genomes]
rs28370409	1.00[EUR][1000 genomes]
rs28432762	1.00[EUR][1000 genomes]
rs28485573	1.00[EUR][1000 genomes]
rs28496972	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28503874	1.00[EUR][1000 genomes]
rs28525412	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28536669	0.98[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28556575	1.00[EUR][1000 genomes]
rs28623761	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28787088	1.00[EUR][1000 genomes]
rs28875276	1.00[EUR][1000 genomes]
rs56228324	1.00[EUR][1000 genomes]
rs57341113	1.00[EUR][1000 genomes]
rs57519708	1.00[EUR][1000 genomes]
rs58743779	0.90[EUR][1000 genomes]
rs60290674	1.00[EUR][1000 genomes]
rs60838421	0.90[EUR][1000 genomes]
rs61293092	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61499746	0.90[EUR][1000 genomes]
rs6468295	1.00[EUR][1000 genomes]
rs6989444	1.00[EUR][1000 genomes]
rs6995738	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6999531	1.00[EUR][1000 genomes]
rs7003487	0.90[EUR][1000 genomes]
rs7011097	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7014562	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7813448	1.00[EUR][1000 genomes]
rs7813623	1.00[EUR][1000 genomes]
rs7816316	0.98[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7818107	1.00[EUR][1000 genomes]
rs7818290	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7818422	1.00[EUR][1000 genomes]
rs7826595	1.00[EUR][1000 genomes]
rs7829892	1.00[EUR][1000 genomes]
rs7837025	1.00[EUR][1000 genomes]
rs7837932	1.00[EUR][1000 genomes]
rs7845212	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3693375	chr8:34631970-34780509	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv972208	chr8:34644254-34790092	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv890716	chr8:34707436-34822797	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1017085	chr8:34742896-35594241	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv539546	chr8:34742896-35594241	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34769200-34770200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:34769800-34778000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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