Variant report

Variant	rs9315474
Chromosome Location	chr13:37780724-37780725
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10507446	0.94[ASN][1000 genomes]
rs11147638	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1324026	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1324027	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1324028	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1324031	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1324032	0.92[ASN][1000 genomes]
rs1324033	0.92[ASN][1000 genomes]
rs1324035	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1324036	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1324037	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1359212	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1408229	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17055062	0.96[EUR][1000 genomes]
rs17055165	0.92[ASN][1000 genomes]
rs17055167	0.92[ASN][1000 genomes]
rs17224133	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1853578	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1853579	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1853580	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1924451	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1998568	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1998569	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1998570	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2057533	0.92[ASN][1000 genomes]
rs2137588	0.96[EUR][1000 genomes]
rs2137589	0.96[EUR][1000 genomes]
rs2147180	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2147182	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2181793	0.93[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2209243	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2209244	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2224849	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2323441	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2323445	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4245381	0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4245382	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4341644	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4359318	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4414353	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4943453	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4943455	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4943456	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4943457	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4943459	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4943460	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6563520	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8001122	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9315476	0.82[EUR][1000 genomes]
rs9315477	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9532010	0.96[ASN][1000 genomes]
rs9532011	0.96[ASN][1000 genomes]
rs9532019	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9532021	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9547741	0.96[ASN][1000 genomes]
rs9547742	0.96[ASN][1000 genomes]
rs9547747	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9547748	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9547751	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9566193	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9566194	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9566195	0.96[EUR][1000 genomes]
rs9566196	0.94[ASN][1000 genomes]
rs9566199	0.92[ASN][1000 genomes]
rs9576195	0.92[YRI][hapmap]
rs9576209	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9576210	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9576211	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9576212	0.97[EUR][1000 genomes]
rs9576215	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9576216	0.97[EUR][1000 genomes]
rs9576217	0.97[EUR][1000 genomes]
rs9576218	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9576219	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9576221	0.94[ASN][1000 genomes]
rs9576222	0.94[ASN][1000 genomes]
rs9576223	0.94[ASN][1000 genomes]
rs9576227	0.92[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	nsv948975	chr13:37281203-38280430	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 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	chr13:37773200-37783600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr13:37777000-37781400	Weak transcription	Osteobl	bone
3	chr13:37777400-37783200	Weak transcription	NHDF-Ad	bronchial
4	chr13:37777600-37781400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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