Variant report

Variant	rs4665149
Chromosome Location	chr2:160924310-160924311
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10454740	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10803761	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11887337	0.85[ASN][1000 genomes]
rs12692582	0.82[ASN][1000 genomes]
rs12999707	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13031600	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13394776	0.86[ASN][1000 genomes]
rs1457233	0.82[ASN][1000 genomes]
rs1457241	0.82[ASN][1000 genomes]
rs2357773	0.86[ASN][1000 genomes]
rs2667031	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2667033	0.85[EUR][1000 genomes]
rs2715929	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4129787	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4233679	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4233680	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4324285	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4368286	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4399677	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4665155	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6432582	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6432587	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6432590	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6432593	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6432603	0.82[ASN][1000 genomes]
rs6720128	0.81[ASN][1000 genomes]
rs6729540	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6749513	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6752593	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6761082	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7558852	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7583743	0.86[ASN][1000 genomes]
rs7608152	0.87[ASN][1000 genomes]
rs996112	0.82[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:160921000-160930200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr2:160921600-160926000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:160922600-160925400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:160922600-160928000	Weak transcription	Fetal Intestine Large	intestine

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