Variant report

Variant	rs9833713
Chromosome Location	chr3:159322692-159322693
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10154893	0.91[CHB][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs1030882	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11921824	0.85[JPT][hapmap]
rs11921827	0.86[JPT][hapmap]
rs12106839	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12107648	0.90[CHB][hapmap];0.92[JPT][hapmap];0.86[ASN][1000 genomes]
rs13434009	0.93[JPT][hapmap]
rs1343824	0.86[ASN][1000 genomes]
rs1347671	0.91[CHB][hapmap];0.93[JPT][hapmap]
rs1356925	0.90[CHB][hapmap];0.89[ASN][1000 genomes]
rs1356926	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs1356927	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1437519	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1437520	0.90[CHB][hapmap];0.92[JPT][hapmap]
rs16830453	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs16830454	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs16830480	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16830484	0.91[CHB][hapmap];0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs16830510	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16830519	1.00[CHB][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs16830523	0.91[CHB][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs16830534	0.84[ASN][1000 genomes]
rs16830546	0.93[JPT][hapmap];1.00[AMR][1000 genomes]
rs16830575	0.86[JPT][hapmap]
rs16830579	0.86[JPT][hapmap]
rs16830581	0.83[JPT][hapmap]
rs1816621	0.81[CHB][hapmap];0.93[JPT][hapmap]
rs1816622	0.85[JPT][hapmap]
rs1978830	0.86[JPT][hapmap]
rs1978831	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs1980254	0.86[ASN][1000 genomes]
rs2118321	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs28718721	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28743043	0.87[ASN][1000 genomes]
rs2886621	0.86[JPT][hapmap]
rs3930053	0.90[CHB][hapmap]
rs59412427	0.86[ASN][1000 genomes]
rs59556163	0.83[ASN][1000 genomes]
rs61018732	0.86[ASN][1000 genomes]
rs61036525	0.89[ASN][1000 genomes]
rs61373569	0.86[ASN][1000 genomes]
rs6769217	1.00[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs6772245	0.83[JPT][hapmap]
rs6796636	1.00[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs73012253	0.84[ASN][1000 genomes]
rs750688	0.83[JPT][hapmap]
rs7619259	0.90[CHB][hapmap];0.86[ASN][1000 genomes]
rs7625882	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs7629269	0.90[CHB][hapmap];0.82[ASN][1000 genomes]
rs7636120	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs7637524	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7650974	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs7653224	0.90[CHB][hapmap];0.86[ASN][1000 genomes]
rs9290045	0.90[CHB][hapmap];0.88[ASN][1000 genomes]
rs9809076	0.85[JPT][hapmap]
rs9809681	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9814630	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs9817830	0.91[CHB][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs9818110	0.82[ASN][1000 genomes]
rs9819000	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs9819080	0.91[CHB][hapmap];0.93[JPT][hapmap];0.84[ASN][1000 genomes]
rs9823562	0.89[ASN][1000 genomes]
rs9824363	0.90[CHB][hapmap];0.92[JPT][hapmap];0.86[ASN][1000 genomes]
rs9826417	0.93[JPT][hapmap]
rs9829229	0.90[CHB][hapmap];0.82[ASN][1000 genomes]
rs9829310	0.85[JPT][hapmap]
rs9832443	0.89[ASN][1000 genomes]
rs9833762	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs9840484	0.91[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs9842465	0.92[JPT][hapmap]
rs9848763	0.91[CHB][hapmap];0.93[JPT][hapmap]
rs9848897	0.91[CHB][hapmap];0.93[JPT][hapmap]
rs9849705	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9851700	0.86[JPT][hapmap]
rs9852770	0.89[ASN][1000 genomes]
rs9857283	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9860690	1.00[CHB][hapmap];0.86[JPT][hapmap];0.89[ASN][1000 genomes]
rs9864641	0.89[ASN][1000 genomes]
rs9866095	0.90[CHB][hapmap];0.89[ASN][1000 genomes]
rs9867212	0.85[JPT][hapmap]
rs9870872	0.84[ASN][1000 genomes]
rs9871188	0.84[ASN][1000 genomes]
rs9877425	0.85[JPT][hapmap]
rs9879792	0.83[JPT][hapmap]
rs9881499	0.91[CHB][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs9881603	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9882328	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs9882993	1.00[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs9883498	0.91[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998949	chr3:158774806-159394550	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 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	chr3:159321200-159322800	Enhancers	NHDF-Ad	bronchial
2	chr3:159321600-159323400	Enhancers	Fetal Heart	heart
3	chr3:159322400-159327200	Weak transcription	NH-A	brain
4	chr3:159322600-159327200	Weak transcription	Osteobl	bone

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