Variant report

Variant	rs9475318
Chromosome Location	chr6:55358360-55358361
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10948936	0.88[YRI][hapmap]
rs12209478	0.81[AFR][1000 genomes]
rs13206666	0.82[JPT][hapmap];0.84[YRI][hapmap]
rs13213275	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3800027	0.84[YRI][hapmap]
rs3807019	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4236132	0.82[AFR][1000 genomes]
rs4320370	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4404773	0.88[AFR][1000 genomes]
rs4496787	0.82[AFR][1000 genomes]
rs4537142	0.82[JPT][hapmap];0.84[YRI][hapmap]
rs4538708	0.86[AFR][1000 genomes]
rs4599641	0.91[AFR][1000 genomes]
rs6459081	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6459082	0.82[AFR][1000 genomes]
rs6914087	0.82[AFR][1000 genomes]
rs6925488	0.82[AFR][1000 genomes]
rs6928264	0.82[AFR][1000 genomes]
rs6936172	0.82[AFR][1000 genomes]
rs7739933	0.87[EUR][1000 genomes]
rs7740208	0.82[AFR][1000 genomes]
rs7744986	0.82[AFR][1000 genomes]
rs7745290	0.82[AFR][1000 genomes]
rs7749276	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7756162	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7756201	0.92[AFR][1000 genomes]
rs7760065	0.82[AFR][1000 genomes]
rs9367638	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9382497	0.82[AFR][1000 genomes]
rs9464254	0.82[AFR][1000 genomes]
rs9475314	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9475333	0.82[AFR][1000 genomes]
rs9475335	0.82[AFR][1000 genomes]
rs9475336	0.82[AFR][1000 genomes]
rs9475337	0.82[AFR][1000 genomes]
rs9475339	0.82[AFR][1000 genomes]
rs9791304	0.81[AFR][1000 genomes]
rs9791308	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034037	chr6:55222409-56069600	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv470819	chr6:55236937-55368815	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1031179	chr6:55237283-55372905	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1029436	chr6:55237283-55386038	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1028560	chr6:55237723-55378113	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1024550	chr6:55237723-55387481	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv462948	chr6:55238091-55368815	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv603163	chr6:55238091-55368815	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1025276	chr6:55349638-55374178	Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	inside rSNPs	diseases
10	nsv948358	chr6:55351282-55477277	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island 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	chr6:55358200-55359200	Weak transcription	NHEK	skin

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