Variant report

Variant	rs9920513
Chromosome Location	chr15:60625325-60625326
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1033027	0.91[ASN][1000 genomes]
rs10851676	0.97[ASN][1000 genomes]
rs10851678	0.83[ASN][1000 genomes]
rs10851679	0.85[ASN][1000 genomes]
rs11071519	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11631793	0.81[ASN][1000 genomes]
rs11631850	0.81[ASN][1000 genomes]
rs11634259	0.81[ASN][1000 genomes]
rs11854079	0.86[ASN][1000 genomes]
rs12439973	0.84[ASN][1000 genomes]
rs12441980	0.81[ASN][1000 genomes]
rs12708462	0.94[ASN][1000 genomes]
rs12898604	0.82[ASN][1000 genomes]
rs12899562	0.95[ASN][1000 genomes]
rs12904910	0.83[ASN][1000 genomes]
rs1551349	0.97[ASN][1000 genomes]
rs1567408	0.90[ASN][1000 genomes]
rs1967370	0.81[ASN][1000 genomes]
rs2014953	0.91[ASN][1000 genomes]
rs2063322	0.91[ASN][1000 genomes]
rs2063324	0.91[ASN][1000 genomes]
rs2063325	0.91[ASN][1000 genomes]
rs2085037	0.83[ASN][1000 genomes]
rs2123828	0.83[ASN][1000 genomes]
rs2136553	0.94[ASN][1000 genomes]
rs2136555	0.94[ASN][1000 genomes]
rs2168013	0.81[ASN][1000 genomes]
rs2175187	0.93[ASN][1000 genomes]
rs2202920	0.91[ASN][1000 genomes]
rs2414667	0.96[ASN][1000 genomes]
rs2414668	1.00[ASN][1000 genomes]
rs2414670	1.00[ASN][1000 genomes]
rs3743269	0.86[ASN][1000 genomes]
rs3743270	0.86[ASN][1000 genomes]
rs3825957	0.86[ASN][1000 genomes]
rs4485290	0.99[ASN][1000 genomes]
rs4530072	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4775257	0.90[ASN][1000 genomes]
rs6494191	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7165592	0.96[ASN][1000 genomes]
rs7167571	0.83[ASN][1000 genomes]
rs7170178	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7170421	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7172784	1.00[ASN][1000 genomes]
rs7176280	0.87[ASN][1000 genomes]
rs7178033	1.00[ASN][1000 genomes]
rs7179548	0.97[ASN][1000 genomes]
rs7180174	0.83[ASN][1000 genomes]
rs8027359	1.00[ASN][1000 genomes]
rs8029375	0.81[ASN][1000 genomes]
rs8033896	0.94[ASN][1000 genomes]
rs8039867	0.94[ASN][1000 genomes]
rs9920432	0.94[ASN][1000 genomes]
rs9920684	0.99[ASN][1000 genomes]
rs9920735	0.94[ASN][1000 genomes]
rs9920883	0.90[ASN][1000 genomes]
rs9972449	0.86[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	esv20296	chr15:60623455-60632031	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:60621600-60627600	Weak transcription	NHDF-Ad	bronchial
2	chr15:60621800-60627600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr15:60623200-60639400	Weak transcription	Fetal Heart	heart

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