Variant report

Variant	rs10503682
Chromosome Location	chr8:20434744-20434745
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10464996	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs10503684	1.00[AFR][1000 genomes]
rs12056831	1.00[AFR][1000 genomes]
rs1351381	0.97[EUR][1000 genomes]
rs1376004	1.00[AFR][1000 genomes]
rs1383248	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17092434	1.00[AFR][1000 genomes]
rs17092692	0.87[EUR][1000 genomes]
rs17092696	0.87[EUR][1000 genomes]
rs17092697	0.87[EUR][1000 genomes]
rs17092700	0.87[EUR][1000 genomes]
rs17092702	0.87[EUR][1000 genomes]
rs17092705	0.89[EUR][1000 genomes]
rs17092707	0.89[EUR][1000 genomes]
rs17092733	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs17419795	1.00[AFR][1000 genomes]
rs17420434	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs17420448	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17420455	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17420595	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17420602	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17491153	1.00[AFR][1000 genomes]
rs17492344	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17492491	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17492862	1.00[AFR][1000 genomes]
rs17603878	1.00[AFR][1000 genomes]
rs17603885	1.00[AFR][1000 genomes]
rs1947258	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs1979430	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1979431	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1979432	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2167173	1.00[AFR][1000 genomes]
rs2898510	1.00[ASN][1000 genomes]
rs4610764	1.00[AFR][1000 genomes]
rs4921713	1.00[AFR][1000 genomes]
rs4922189	1.00[AFR][1000 genomes]
rs4922200	1.00[AFR][1000 genomes]
rs4922210	1.00[AFR][1000 genomes]
rs6989281	1.00[AFR][1000 genomes]
rs6994255	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs6999584	1.00[AFR][1000 genomes]
rs6999736	1.00[AFR][1000 genomes]
rs7011434	0.82[EUR][1000 genomes]
rs73614170	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73626736	0.84[EUR][1000 genomes]
rs7465534	1.00[AFR][1000 genomes]
rs7816876	1.00[ASN][1000 genomes]
rs7830125	1.00[AFR][1000 genomes]
rs7845060	1.00[AFR][1000 genomes]
rs950511	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033511	chr8:19751299-20625091	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv530877	chr8:19873053-20593254	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	esv2758152	chr8:20228949-20514807	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2759603	chr8:20228949-20514807	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv469890	chr8:20239114-20445136	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv482881	chr8:20239114-20445136	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv916454	chr8:20342959-20531705	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20433800-20435200	Enhancers	Fetal Kidney	kidney
2	chr8:20434000-20435200	Enhancers	Fetal Stomach	stomach
3	chr8:20434000-20435400	Enhancers	Fetal Lung	lung
4	chr8:20434600-20435000	Flanking Active TSS	Liver	Liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links