Variant report

Variant	rs10021663
Chromosome Location	chr4:149870546-149870547
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs13127141	0.82[ASN][1000 genomes]
rs1357440	0.84[ASN][1000 genomes]
rs1403455	0.82[ASN][1000 genomes]
rs1474304	0.86[ASN][1000 genomes]
rs1523012	0.85[ASN][1000 genomes]
rs1523013	0.84[ASN][1000 genomes]
rs1523014	0.84[ASN][1000 genomes]
rs1523015	0.84[ASN][1000 genomes]
rs1523016	0.84[ASN][1000 genomes]
rs1523017	0.84[ASN][1000 genomes]
rs1634070	0.84[ASN][1000 genomes]
rs1634071	0.84[ASN][1000 genomes]
rs1634082	0.86[ASN][1000 genomes]
rs1634083	0.86[ASN][1000 genomes]
rs1634097	0.92[ASN][1000 genomes]
rs1719678	0.91[ASN][1000 genomes]
rs1719683	0.85[ASN][1000 genomes]
rs1719684	0.86[ASN][1000 genomes]
rs17584189	0.81[ASN][1000 genomes]
rs17623254	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17721605	0.81[ASN][1000 genomes]
rs1916243	0.81[ASN][1000 genomes]
rs2103065	0.81[ASN][1000 genomes]
rs2358680	0.92[ASN][1000 genomes]
rs2520496	0.91[ASN][1000 genomes]
rs4240350	0.82[ASN][1000 genomes]
rs4240351	0.82[ASN][1000 genomes]
rs4240352	0.94[ASN][1000 genomes]
rs4835147	0.92[ASN][1000 genomes]
rs4835546	0.81[ASN][1000 genomes]
rs4835549	0.95[ASN][1000 genomes]
rs538951	0.81[ASN][1000 genomes]
rs541498	0.82[ASN][1000 genomes]
rs58528421	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6535645	0.90[ASN][1000 genomes]
rs6828358	0.82[ASN][1000 genomes]
rs6846355	0.92[ASN][1000 genomes]
rs6858768	0.92[ASN][1000 genomes]
rs72719803	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72737816	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7668071	0.92[ASN][1000 genomes]
rs7682891	0.92[ASN][1000 genomes]
rs7695802	0.81[ASN][1000 genomes]
rs7697941	0.81[ASN][1000 genomes]
rs853695	0.89[ASN][1000 genomes]
rs853705	0.86[ASN][1000 genomes]
rs853707	0.88[ASN][1000 genomes]
rs853708	0.90[ASN][1000 genomes]
rs853709	0.86[ASN][1000 genomes]
rs853728	0.92[ASN][1000 genomes]
rs853730	0.92[ASN][1000 genomes]
rs853731	0.92[ASN][1000 genomes]
rs860501	0.86[ASN][1000 genomes]
rs860502	0.87[ASN][1000 genomes]
rs860503	0.88[ASN][1000 genomes]
rs861225	0.83[ASN][1000 genomes]
rs862655	0.91[ASN][1000 genomes]
rs862656	0.91[ASN][1000 genomes]
rs862658	0.81[ASN][1000 genomes]
rs864093	0.92[ASN][1000 genomes]
rs9307850	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv461677	chr4:149794284-149903982	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv595686	chr4:149794284-149903982	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv470083	chr4:149817052-149903982	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:149867400-149871200	Weak transcription	Fetal Brain Male	brain

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