Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10134005	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10137608	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10146035	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10148642	0.96[ASN][1000 genomes]
rs10150745	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17119896	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17707121	0.96[ASN][1000 genomes]
rs28399118	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs28446157	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3935697	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4075208	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4277275	0.96[ASN][1000 genomes]
rs4277283	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55986944	0.96[ASN][1000 genomes]
rs7142508	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7143199	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs8005901	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs8009583	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs8012329	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs8019836	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832845	chr14:84726378-84900199	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84776200-84778400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr14:84777800-84780200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:84778200-84778800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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