Variant report

Variant	rs9826417
Chromosome Location	chr3:159356482-159356483
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10154893	0.86[JPT][hapmap]
rs11921824	0.89[CHB][hapmap];0.93[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11921827	0.89[CHB][hapmap];0.93[JPT][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12107648	0.84[JPT][hapmap]
rs13434009	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1347671	0.86[JPT][hapmap];0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1347672	1.00[CHB][hapmap];0.84[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1356927	0.93[JPT][hapmap]
rs1437519	0.92[JPT][hapmap]
rs1437520	0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs16830510	0.93[JPT][hapmap]
rs16830519	0.86[JPT][hapmap]
rs16830523	0.86[JPT][hapmap]
rs16830546	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs16830575	0.89[CHB][hapmap];0.93[JPT][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16830579	0.89[CHB][hapmap];0.93[JPT][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16830581	0.88[CHB][hapmap];0.92[JPT][hapmap];0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16830589	0.88[CHB][hapmap];0.84[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1816621	0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs1816622	1.00[CHB][hapmap];0.93[JPT][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1962890	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1978830	1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28434644	0.91[ASN][1000 genomes]
rs2886621	1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4494974	0.83[ASN][1000 genomes]
rs6772245	1.00[CHB][hapmap];0.92[JPT][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs750688	1.00[CHB][hapmap];0.92[JPT][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7637524	0.83[ASN][1000 genomes]
rs9290046	0.88[CHB][hapmap];0.84[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9290047	0.89[CHB][hapmap];0.86[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9809076	0.89[CHB][hapmap];0.93[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9809681	0.93[JPT][hapmap]
rs9819000	0.92[JPT][hapmap];0.90[ASN][1000 genomes]
rs9819080	0.86[JPT][hapmap]
rs9824363	0.84[JPT][hapmap]
rs9829310	1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9832970	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9833713	0.93[JPT][hapmap]
rs9842465	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9848763	0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs9848897	0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs9849705	0.90[ASN][1000 genomes]
rs9851700	0.89[CHB][hapmap];0.93[JPT][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9857283	0.85[ASN][1000 genomes]
rs9860690	0.88[CHB][hapmap]
rs9867212	0.89[CHB][hapmap];0.93[JPT][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9877425	0.89[CHB][hapmap];0.93[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9879792	0.88[CHB][hapmap];0.92[JPT][hapmap];0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9881603	0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs9882328	0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs9883498	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]

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:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:159350600-159358200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr3:159353000-159358000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr3:159353200-159358000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr3:159353200-159358000	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr3:159353200-159358000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:159353200-159358200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr3:159355800-159356600	Enhancers	HMEC	breast
8	chr3:159356200-159363200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr3:159356400-159379800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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