Variant report

Variant	rs11990050
Chromosome Location	chr8:51301703-51301704
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11984847	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11985543	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11988078	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11988109	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11988505	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11988866	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11988979	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11989227	0.83[YRI][hapmap];0.84[AFR][1000 genomes]
rs11990082	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11990159	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11991343	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11993522	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11995178	1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11996964	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11997407	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16914775	0.83[YRI][hapmap];0.84[AFR][1000 genomes]
rs56804531	0.85[AFR][1000 genomes]
rs56822119	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56890895	0.85[AFR][1000 genomes]
rs57722611	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58233516	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58747692	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59960463	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60273928	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60478315	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61384064	1.00[AFR][1000 genomes];1.00[AMR][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	nsv916392	chr8:50827638-51395140	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv948436	chr8:51115028-51917504	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv831312	chr8:51239772-51422844	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51300000-51319800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr8:51301400-51301800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:51301400-51301800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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