Variant report

Variant	rs10851073
Chromosome Location	chr13:98237608-98237609
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs12869921	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12870589	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1304392	0.81[MEX][hapmap]
rs184729	0.86[ASN][1000 genomes]
rs184731	0.88[ASN][1000 genomes]
rs1854225	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1854227	0.82[EUR][1000 genomes]
rs1887561	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2094474	0.89[ASN][1000 genomes]
rs2389861	0.97[ASN][1000 genomes]
rs2389909	0.82[CHB][hapmap]
rs2769280	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2769283	0.81[ASN][1000 genomes]
rs2770229	0.89[ASN][1000 genomes]
rs4346086	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4400904	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4534691	0.89[ASN][1000 genomes]
rs4771275	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4771276	0.95[ASN][1000 genomes]
rs4772004	0.89[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7139828	0.88[ASN][1000 genomes]
rs7338682	0.88[ASN][1000 genomes]
rs787467	0.87[ASN][1000 genomes]
rs7981655	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7982432	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9300422	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9513256	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9516953	0.83[EUR][1000 genomes]
rs9516959	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9516961	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9516962	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9516963	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9516967	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9516974	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9516977	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9516978	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9556743	0.94[ASN][1000 genomes]
rs9556744	0.93[ASN][1000 genomes]
rs9556745	0.95[ASN][1000 genomes]
rs9556748	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9556751	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9556752	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9556759	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9556760	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9556761	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9556762	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9584602	0.94[ASN][1000 genomes]
rs9584604	0.88[ASN][1000 genomes]
rs9634497	0.94[ASN][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	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
3	nsv900940	chr13:98225221-98281637	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv900941	chr13:98230575-98267751	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1140	chr13:98233230-98278197	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:98235600-98237800	Enhancers	HepG2	liver
2	chr13:98236000-98237800	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr13:98237000-98238000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr13:98237000-98240200	Weak transcription	Fetal Heart	heart
5	chr13:98237200-98238000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:98237400-98239000	Weak transcription	Fetal Intestine Large	intestine

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