Variant report

Variant	rs4505006
Chromosome Location	chr10:52915469-52915470
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10995918	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1871630	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1904676	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1904677	0.93[ASN][1000 genomes]
rs1904683	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1904687	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1904688	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1904689	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1904692	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1904693	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1904695	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1904696	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1904697	0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs1904699	0.80[JPT][hapmap]
rs2339731	0.93[ASN][1000 genomes]
rs2339732	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3851088	0.93[ASN][1000 genomes]
rs3862576	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3862579	0.91[ASN][1000 genomes]
rs3998228	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6479991	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7068022	0.94[ASN][1000 genomes]
rs7085697	0.93[ASN][1000 genomes]
rs7893773	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9414844	0.93[ASN][1000 genomes]
rs9415733	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9633538	0.86[JPT][hapmap];0.83[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	nsv1036645	chr10:52804961-53159076	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52895200-52924000	Weak transcription	Fetal Stomach	stomach
2	chr10:52895600-52916600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr10:52898000-52919600	Weak transcription	NHLF	lung
4	chr10:52906000-52931200	Weak transcription	Fetal Muscle Leg	muscle
5	chr10:52907200-52916800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:52908000-52929600	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr10:52908400-52916800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr10:52908400-52929600	Weak transcription	Aorta	Aorta
9	chr10:52910000-52931000	Weak transcription	Fetal Lung	lung
10	chr10:52910600-52942400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr10:52913000-52922000	Weak transcription	Right Ventricle	heart
12	chr10:52913200-52921800	Weak transcription	Colon Smooth Muscle	Colon

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