Variant report

Variant	rs10154893
Chromosome Location	chr3:159327510-159327511
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs11921824	0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs11921827	0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs12107648	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs13434009	0.86[JPT][hapmap]
rs1343824	0.96[ASN][1000 genomes]
rs1347671	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1347672	0.84[JPT][hapmap]
rs1356925	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1356926	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs1356927	0.91[CHB][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs1437519	0.90[CHB][hapmap];0.92[JPT][hapmap];0.84[ASN][1000 genomes]
rs1437520	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1550218	1.00[CEU][hapmap]
rs1581342	0.86[JPT][hapmap]
rs16830484	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16830487	1.00[CEU][hapmap]
rs16830507	1.00[CEU][hapmap]
rs16830510	1.00[CEU][hapmap];0.91[CHB][hapmap];0.93[JPT][hapmap];0.90[YRI][hapmap];0.84[AFR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16830519	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16830523	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16830534	0.98[ASN][1000 genomes]
rs16830546	0.86[JPT][hapmap]
rs16830575	0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs16830579	0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs16830581	0.92[JPT][hapmap]
rs16830589	0.84[JPT][hapmap]
rs1816621	0.91[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1962890	0.83[ASN][1000 genomes]
rs1976819	1.00[CEU][hapmap]
rs1978830	0.93[JPT][hapmap]
rs1978831	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs1980254	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2118321	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs28434644	0.84[ASN][1000 genomes]
rs28743043	1.00[ASN][1000 genomes]
rs2886621	0.93[JPT][hapmap]
rs3930053	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs4494974	0.93[ASN][1000 genomes]
rs59412427	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59556163	0.96[ASN][1000 genomes]
rs60665389	0.91[ASN][1000 genomes]
rs61018732	0.96[ASN][1000 genomes]
rs61036525	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61373569	0.96[ASN][1000 genomes]
rs6769217	1.00[CEU][hapmap];0.91[CHB][hapmap];0.88[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6772245	0.92[JPT][hapmap]
rs6796636	1.00[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73012253	0.98[ASN][1000 genomes]
rs750688	0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs7619259	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7625882	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs7629269	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7636120	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap]
rs7637524	0.89[ASN][1000 genomes]
rs7650974	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs7653224	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9290045	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.89[ASN][1000 genomes]
rs9290046	0.84[JPT][hapmap]
rs9290047	0.86[JPT][hapmap]
rs9809076	0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs9809681	0.91[CHB][hapmap];0.93[JPT][hapmap]
rs9817830	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9818110	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9819000	0.90[CHB][hapmap];0.92[JPT][hapmap];0.85[ASN][1000 genomes]
rs9819080	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs9823562	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9824363	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs9826417	0.86[JPT][hapmap]
rs9829229	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9829310	0.93[JPT][hapmap]
rs9832443	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9832970	0.84[ASN][1000 genomes]
rs9833614	1.00[CEU][hapmap];0.86[JPT][hapmap]
rs9833713	0.91[CHB][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs9833762	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs9840484	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9842465	0.84[JPT][hapmap]
rs9848763	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9848897	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9849705	0.85[ASN][1000 genomes]
rs9851700	0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs9852770	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9857283	0.90[ASN][1000 genomes]
rs9860690	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9864641	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9866095	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9867212	0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs9870872	0.98[ASN][1000 genomes]
rs9871188	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9877425	0.93[JPT][hapmap]
rs9879792	0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs9881499	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9881603	0.90[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs9882328	0.91[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9882993	1.00[CEU][hapmap];0.91[CHB][hapmap];0.88[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9883498	0.83[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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:159325600-159327800	Enhancers	Fetal Heart	heart
2	chr3:159327000-159328000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr3:159327200-159327600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr3:159327200-159328000	Enhancers	Osteobl	bone
5	chr3:159327200-159328200	Enhancers	NH-A	brain

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