Variant report

Variant	rs58269079
Chromosome Location	chr2:53063545-53063546
allele	G/T
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:34)

rs_ID	r²[population]
rs1011228	0.82[ASN][1000 genomes]
rs10490579	0.81[EUR][1000 genomes]
rs10490583	0.82[EUR][1000 genomes]
rs12470339	0.80[ASN][1000 genomes]
rs17043472	0.82[EUR][1000 genomes]
rs17043496	0.82[EUR][1000 genomes]
rs17043734	0.81[EUR][1000 genomes]
rs17043739	0.81[EUR][1000 genomes]
rs17043781	0.81[EUR][1000 genomes]
rs17571144	0.81[EUR][1000 genomes]
rs2116006	0.81[EUR][1000 genomes]
rs34049687	0.86[EUR][1000 genomes]
rs41392646	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56286124	0.81[EUR][1000 genomes]
rs59711835	0.88[ASN][1000 genomes]
rs62128173	0.82[EUR][1000 genomes]
rs62128174	0.82[EUR][1000 genomes]
rs62128203	0.85[EUR][1000 genomes]
rs62128205	0.86[EUR][1000 genomes]
rs62138246	0.81[EUR][1000 genomes]
rs62138247	0.81[EUR][1000 genomes]
rs62138248	0.81[EUR][1000 genomes]
rs62138249	0.81[EUR][1000 genomes]
rs62138250	0.81[EUR][1000 genomes]
rs62140275	0.81[EUR][1000 genomes]
rs62140277	0.81[EUR][1000 genomes]
rs62140278	0.81[EUR][1000 genomes]
rs62140279	0.81[EUR][1000 genomes]
rs62140283	0.81[EUR][1000 genomes]
rs62140284	0.81[EUR][1000 genomes]
rs62140285	0.81[EUR][1000 genomes]
rs725865	0.82[EUR][1000 genomes]
rs72808329	0.80[EUR][1000 genomes]
rs72808339	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998380	chr2:52891706-53222155	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	esv2763631	chr2:52910862-53169629	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1006244	chr2:52958322-53169617	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1005813	chr2:52959769-53114865	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1010978	chr2:52959769-53249951	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1014068	chr2:52960353-53169617	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv520722	chr2:53039770-53421015	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53063200-53066000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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