Variant report

Variant	rs9630200
Chromosome Location	chr11:120575845-120575846
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs11217978	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11217979	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11217980	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11217981	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11217983	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11217984	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11217987	0.90[CEU][hapmap];0.82[CHB][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11217988	0.90[CEU][hapmap];0.80[YRI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11217989	0.90[CEU][hapmap];0.85[EUR][1000 genomes]
rs11603713	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11604327	1.00[CHB][hapmap];0.88[JPT][hapmap];0.92[ASN][1000 genomes]
rs12270261	0.89[CEU][hapmap]
rs12270409	0.90[CEU][hapmap];0.82[CHB][hapmap];0.80[AMR][1000 genomes]
rs12272864	0.89[CEU][hapmap]
rs12274300	0.90[CEU][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12276408	0.92[CHB][hapmap];0.89[EUR][1000 genomes]
rs12276440	1.00[CEU][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12278795	0.89[CEU][hapmap]
rs12280296	0.89[CEU][hapmap]
rs12281464	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12281614	0.85[EUR][1000 genomes]
rs12291927	0.89[CEU][hapmap]
rs12293393	0.89[CEU][hapmap]
rs12294858	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12295113	0.89[CEU][hapmap]
rs12295200	0.89[CEU][hapmap]
rs17124211	1.00[CEU][hapmap];0.86[CHB][hapmap]
rs17124222	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2846109	0.89[CEU][hapmap]
rs2852225	0.89[CEU][hapmap]
rs2852227	0.89[CEU][hapmap]
rs28781001	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34463064	0.82[ASN][1000 genomes]
rs4451741	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs4567478	0.90[CEU][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61355898	0.94[ASN][1000 genomes]
rs61901379	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61901380	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61902688	0.80[AMR][1000 genomes]
rs7102869	0.89[CEU][hapmap]
rs7103021	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7103228	0.90[CEU][hapmap]
rs7103418	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7119619	0.90[CEU][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7946325	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9630199	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9630201	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[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	nsv1054407	chr11:120535570-120630114	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1053607	chr11:120540795-120802006	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3693392	chr11:120549745-120628012	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120568000-120580600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr11:120570000-120581600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:120570200-120577400	Weak transcription	Fetal Lung	lung
4	chr11:120574200-120576000	Weak transcription	Brain Angular Gyrus	brain
5	chr11:120575200-120577800	Weak transcription	Ovary	ovary

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links