Variant report

Variant	rs1459796
Chromosome Location	chr1:72225877-72225878
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11209837	0.82[ASN][1000 genomes]
rs11584866	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12023733	0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12023757	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12024388	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12030035	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12031657	0.82[EUR][1000 genomes]
rs12039538	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12041607	0.82[EUR][1000 genomes]
rs12048869	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17091758	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1870523	0.82[ASN][1000 genomes]
rs1870524	0.82[ASN][1000 genomes]
rs1870525	0.82[ASN][1000 genomes]
rs57227393	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs57839383	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs59851000	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6424442	0.82[EUR][1000 genomes]
rs6424447	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6671557	0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6697370	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6701156	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72944111	0.82[EUR][1000 genomes]
rs72944128	0.92[EUR][1000 genomes]
rs72944129	0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72944192	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72946013	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72946022	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72946034	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72948021	0.89[EUR][1000 genomes]
rs7528030	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7531512	0.82[EUR][1000 genomes]
rs7541406	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7546909	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949599	chr1:71655652-72327802	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1007250	chr1:71998391-72350683	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv534992	chr1:71998391-72350683	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv948821	chr1:72049987-72477221	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1003446	chr1:72060680-72419918	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv461884	chr1:72077549-72238691	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv546476	chr1:72077549-72238691	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv817447	chr1:72098815-72558020	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1008210	chr1:72099161-72374197	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv533779	chr1:72124095-72241965	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv830181	chr1:72155983-72296578	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv916783	chr1:72196061-72707953	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72225600-72226000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr1:72225600-72226200	Enhancers	HUVEC	blood vessel

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links