Variant report

Variant	rs9920735
Chromosome Location	chr15:60625850-60625851
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1033027	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10851676	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10851679	0.84[ASN][1000 genomes]
rs11071519	0.94[ASN][1000 genomes]
rs12439973	0.80[EUR][1000 genomes]
rs12708462	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12899562	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1551349	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1567408	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1967370	0.81[EUR][1000 genomes]
rs2014953	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2063322	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2063324	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2063325	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2136553	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2136555	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2175187	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2202920	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2414667	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2414668	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2414670	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4485290	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4530072	0.91[ASN][1000 genomes]
rs4775257	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6494191	0.91[ASN][1000 genomes]
rs7165592	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7167571	0.80[EUR][1000 genomes]
rs7170178	0.90[ASN][1000 genomes]
rs7170421	0.90[ASN][1000 genomes]
rs7172784	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7176280	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7178033	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7179548	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8027359	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8033896	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8039867	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9920432	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9920513	0.94[ASN][1000 genomes]
rs9920684	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9920883	0.83[EUR][1000 genomes];0.84[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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