Variant report

Variant	rs9850280
Chromosome Location	chr3:155178247-155178248
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10936004	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11709283	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11709568	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11714606	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12107115	0.91[ASN][1000 genomes]
rs12630784	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12631218	0.90[ASN][1000 genomes]
rs12633188	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12633236	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12633676	0.84[ASN][1000 genomes]
rs12634171	0.90[ASN][1000 genomes]
rs12637360	0.90[ASN][1000 genomes]
rs13074373	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13080233	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13093286	0.86[ASN][1000 genomes]
rs13094738	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2351	0.89[ASN][1000 genomes]
rs2352	0.89[ASN][1000 genomes]
rs28575712	0.89[ASN][1000 genomes]
rs35259851	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35630673	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs36006137	0.84[ASN][1000 genomes]
rs4679745	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4679746	0.90[ASN][1000 genomes]
rs4679747	0.90[ASN][1000 genomes]
rs4680180	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4680181	0.90[ASN][1000 genomes]
rs4680182	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4680183	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4680185	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56103965	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6440990	0.90[ASN][1000 genomes]
rs6440993	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6440994	0.87[ASN][1000 genomes]
rs6440995	0.86[ASN][1000 genomes]
rs6798100	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6802079	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6804318	0.89[ASN][1000 genomes]
rs7616618	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7616703	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7618495	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7643640	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9289955	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9809653	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9818939	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9829532	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9848852	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9856512	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9869956	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9870325	0.96[EUR][1000 genomes];0.96[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	nsv1000753	chr3:154848433-155207022	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv536773	chr3:154848433-155207022	Enhancers Strong transcription Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv877679	chr3:155128968-155204939	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155166800-155178800	Weak transcription	Pancreas	Pancrea
2	chr3:155170000-155179000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:155172400-155179400	Weak transcription	Dnd41	blood
4	chr3:155173800-155182400	Weak transcription	Gastric	stomach
5	chr3:155175000-155183000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr3:155176000-155183400	Weak transcription	Fetal Intestine Small	intestine
7	chr3:155177600-155186800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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