Variant report

Variant	rs924517
Chromosome Location	chr3:156981485-156981486
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:156974074..156978072-chr3:156979844..156983022,4	K562	blood:

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10212545	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1027603	0.89[CHB][hapmap]
rs10451916	0.87[MEX][hapmap];0.84[TSI][hapmap];0.80[EUR][1000 genomes]
rs1046938	0.91[MEX][hapmap];0.84[TSI][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10513507	0.83[EUR][1000 genomes]
rs10936085	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs11926167	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12496879	0.89[CHB][hapmap]
rs12629549	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12696045	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13061214	0.80[CEU][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13081036	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13081038	0.87[MEX][hapmap];0.84[TSI][hapmap];0.80[EUR][1000 genomes]
rs13084522	0.85[EUR][1000 genomes]
rs1392799	0.87[MEX][hapmap];0.84[TSI][hapmap];0.80[EUR][1000 genomes]
rs1403103	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1403104	0.80[TSI][hapmap]
rs1500916	0.83[CHB][hapmap]
rs1500920	0.94[CHB][hapmap]
rs1500925	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1546261	0.89[CHB][hapmap]
rs1568609	0.89[CHB][hapmap]
rs1568612	0.94[CHB][hapmap];0.80[ASN][1000 genomes]
rs1587534	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1587535	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1608127	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs16827350	0.81[EUR][1000 genomes]
rs16827384	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2047649	0.83[CHB][hapmap]
rs2088814	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2088815	0.88[CHB][hapmap]
rs2133952	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28384296	0.85[EUR][1000 genomes]
rs3749214	0.83[MEX][hapmap];0.84[TSI][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4368452	0.90[EUR][1000 genomes]
rs4563363	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4632503	0.81[EUR][1000 genomes]
rs4680342	0.85[CEU][hapmap]
rs4680346	0.81[EUR][1000 genomes]
rs4680348	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4680351	0.94[CHB][hapmap];0.80[ASN][1000 genomes]
rs4680359	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs6441121	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6441123	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs67196056	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6773061	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6776647	0.94[CHB][hapmap];0.82[ASN][1000 genomes]
rs6780831	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6783595	0.84[CEU][hapmap]
rs6801110	0.83[CHB][hapmap]
rs6808284	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6808457	0.80[CEU][hapmap];0.80[EUR][1000 genomes]
rs6809003	0.85[CEU][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap]
rs6809394	0.85[CEU][hapmap];0.86[TSI][hapmap]
rs7614339	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs7620178	0.83[AMR][1000 genomes]
rs7625059	0.87[MEX][hapmap];0.84[TSI][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7631556	0.89[CHB][hapmap]
rs7636185	0.81[EUR][1000 genomes]
rs7638194	0.91[MEX][hapmap];0.84[TSI][hapmap];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7642179	0.81[EUR][1000 genomes]
rs7647643	0.87[MEX][hapmap];0.84[TSI][hapmap]
rs9289978	0.80[EUR][1000 genomes]
rs9289979	0.80[EUR][1000 genomes]
rs9289980	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9811195	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9827676	0.80[EUR][1000 genomes]
rs9834771	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9838724	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9849168	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9857875	0.88[CHB][hapmap]
rs9861469	0.80[EUR][1000 genomes]
rs9867618	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs988587	0.83[CHB][hapmap]
rs988588	0.89[CHB][hapmap]
rs9990136	0.89[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829766	chr3:156811536-157020551	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
2	nsv877687	chr3:156924793-157044184	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:156967200-156982000	Weak transcription	Lung	lung
2	chr3:156967200-156989000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr3:156967200-157000000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr3:156967200-157000000	Weak transcription	NH-A	brain
5	chr3:156967200-157007800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:156968000-156981800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr3:156974000-156982400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr3:156977800-156982000	Enhancers	Osteobl	bone
9	chr3:156978200-156981600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr3:156978400-156981600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr3:156979600-156997000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr3:156980400-156981600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr3:156980400-156982400	Enhancers	HUVEC	blood vessel
14	chr3:156981000-156983600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:156981200-156991400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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