Variant report

Variant	rs7047759
Chromosome Location	chr9:104027518-104027519
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10989456	0.85[CHB][hapmap];0.86[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10989462	0.85[CHB][hapmap];0.82[ASN][1000 genomes]
rs12338031	0.90[CHB][hapmap];0.86[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12338159	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12341244	0.83[CHB][hapmap]
rs12341316	0.85[CHB][hapmap];0.83[ASN][1000 genomes]
rs12683367	0.82[ASN][1000 genomes]
rs13289023	0.85[CHB][hapmap];0.83[ASN][1000 genomes]
rs1329073	0.90[CHB][hapmap];0.86[JPT][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1329077	0.85[CHB][hapmap];0.83[ASN][1000 genomes]
rs1329079	0.85[CHB][hapmap];0.83[ASN][1000 genomes]
rs1329089	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs13295287	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13296052	0.85[CHB][hapmap];0.82[ASN][1000 genomes]
rs1367755	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16920100	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs1831235	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2033393	0.82[ASN][1000 genomes]
rs2033394	0.80[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2039128	0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs35870850	0.82[ASN][1000 genomes]
rs36070696	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3944892	0.85[CHB][hapmap];0.82[ASN][1000 genomes]
rs4743454	0.85[CHB][hapmap];0.86[JPT][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4743456	0.82[ASN][1000 genomes]
rs7023477	0.85[CHB][hapmap];0.83[ASN][1000 genomes]
rs7029850	0.95[ASN][1000 genomes]
rs7032821	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs7034058	0.85[CHB][hapmap];0.83[ASN][1000 genomes]
rs7035407	0.85[CHB][hapmap];0.82[ASN][1000 genomes]
rs7044697	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs750662	0.90[CHB][hapmap];0.82[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104026800-104028000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr9:104027200-104031600	Weak transcription	HepG2	liver
3	chr9:104027400-104028000	Enhancers	Fetal Brain Female	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links