Variant report

Variant	rs812010
Chromosome Location	chr13:98211637-98211638
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs173241	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs184729	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs184731	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1854227	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1887561	0.84[EUR][1000 genomes]
rs2094474	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2389861	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2769280	0.84[AMR][1000 genomes]
rs2769283	0.80[AMR][1000 genomes]
rs2770220	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2770229	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4346086	0.81[EUR][1000 genomes]
rs4400904	0.82[EUR][1000 genomes]
rs4534691	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4771275	0.81[EUR][1000 genomes]
rs4771276	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7139828	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7338682	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs787467	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7981655	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7982432	0.81[EUR][1000 genomes]
rs9300422	0.82[EUR][1000 genomes]
rs9516959	0.83[EUR][1000 genomes]
rs9516967	0.81[EUR][1000 genomes]
rs9556742	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9556743	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9556744	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9556745	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9556760	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9556761	0.84[AMR][1000 genomes]
rs9584602	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9634497	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043113	chr13:98136208-98485012	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv541884	chr13:98136208-98485012	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr13:98208000-98212800	Weak transcription	Fetal Brain Male	brain
2	chr13:98208400-98212600	Weak transcription	Fetal Brain Female	brain

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