Variant report

Variant	rs3903111
Chromosome Location	chr9:21264850-21264851
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10114358	0.92[EUR][1000 genomes]
rs10116540	0.90[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs10757199	0.90[JPT][hapmap]
rs10757208	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10811509	0.80[ASN][1000 genomes]
rs10811514	0.94[ASN][1000 genomes]
rs10811519	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10964918	0.82[ASN][1000 genomes]
rs10964928	0.94[ASN][1000 genomes]
rs10964930	0.90[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs10964932	0.90[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs10964933	0.90[ASN][1000 genomes]
rs10964934	0.90[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs10964956	0.82[YRI][hapmap]
rs12551190	0.90[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs12553763	0.90[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs12555631	0.90[JPT][hapmap]
rs1330316	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1330317	0.99[ASN][1000 genomes]
rs1330318	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1330319	0.90[EUR][1000 genomes]
rs1330320	0.91[EUR][1000 genomes]
rs1330322	0.81[CEU][hapmap]
rs1330323	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1330324	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1330325	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1411436	0.90[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs1424854	0.83[JPT][hapmap]
rs1543640	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1590898	1.00[ASN][1000 genomes]
rs1834247	0.91[JPT][hapmap]
rs1928854	0.90[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs1928855	0.94[ASN][1000 genomes]
rs1928856	0.94[ASN][1000 genomes]
rs2015345	0.91[JPT][hapmap]
rs2225329	1.00[ASN][1000 genomes]
rs28437205	0.99[ASN][1000 genomes]
rs4112794	0.96[ASN][1000 genomes]
rs4628333	0.90[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs4978068	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4978069	0.99[ASN][1000 genomes]
rs56035072	0.80[ASN][1000 genomes]
rs57122438	0.96[ASN][1000 genomes]
rs57146220	0.96[ASN][1000 genomes]
rs7024738	0.94[EUR][1000 genomes]
rs7033839	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs7037147	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs7037707	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73418252	0.99[ASN][1000 genomes]
rs7858766	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7872575	0.87[AMR][1000 genomes];0.95[EUR][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	nsv817218	chr9:20687769-21309177	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv892724	chr9:20690244-21517302	Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	153 gene(s)	inside rSNPs	diseases
3	nsv892734	chr9:21108817-21323089	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1035128	chr9:21196300-21269669	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv2761295	chr9:21258108-21281544	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv3447912	chr9:21260652-21290903	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv430006	chr9:21262516-21280782	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs3903111	KLHL9	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21264800-21265400	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr9:21264800-21268600	Enhancers	Breast Myoepithelial Primary Cells	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links