Variant report

Variant	rs72659801
Chromosome Location	chr8:60833616-60833617
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10081579	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10087623	0.98[EUR][1000 genomes]
rs10097767	1.00[ASN][1000 genomes]
rs10098915	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10111058	0.87[ASN][1000 genomes]
rs10957118	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16925420	0.98[EUR][1000 genomes]
rs17271634	0.95[ASN][1000 genomes]
rs1995941	1.00[ASN][1000 genomes]
rs28445557	1.00[ASN][1000 genomes]
rs28626870	1.00[ASN][1000 genomes]
rs28668089	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28673143	0.95[ASN][1000 genomes]
rs28690268	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55827533	0.98[EUR][1000 genomes]
rs57344747	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62512089	0.90[ASN][1000 genomes]
rs6997337	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6998079	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72659716	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72659731	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72659733	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72659760	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72659762	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72659763	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72659765	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72659799	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72659802	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72661403	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72661404	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72661406	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72661410	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72661416	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72661421	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72661426	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72661427	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72661442	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72661445	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72661495	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72663207	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72663214	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72663216	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72663221	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72663222	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72663223	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7833035	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7833043	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7834199	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7837331	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7838137	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9650196	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv831331	chr8:60770382-60959633	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60828600-60834800	Weak transcription	Fetal Stomach	stomach
2	chr8:60828800-60834000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr8:60830000-60834000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr8:60830000-60834200	Enhancers	Primary B cells from peripheral blood	blood
5	chr8:60832800-60834000	Weak transcription	Colon Smooth Muscle	Colon
6	chr8:60833000-60833800	Weak transcription	NHDF-Ad	bronchial
7	chr8:60833000-60833800	Weak transcription	Osteobl	bone
8	chr8:60833000-60834000	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr8:60833000-60834000	Weak transcription	NH-A	brain
10	chr8:60833000-60834200	Enhancers	Primary B cells from cord blood	blood
11	chr8:60833600-60833800	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr8:60833600-60834000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr8:60833600-60835000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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