Variant report

Variant	rs2292300
Chromosome Location	chr2:211167132-211167133
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1074158	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11889646	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs11890217	0.95[ASN][1000 genomes]
rs11904281	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12469767	0.99[ASN][1000 genomes]
rs12999760	0.85[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs13009477	0.92[ASN][1000 genomes]
rs1355204	0.95[ASN][1000 genomes]
rs1472955	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16844288	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1963089	0.98[ASN][1000 genomes]
rs1995835	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs1995836	0.99[ASN][1000 genomes]
rs2048274	0.85[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2048276	0.97[ASN][1000 genomes]
rs2063310	0.99[ASN][1000 genomes]
rs2063311	0.99[ASN][1000 genomes]
rs2136457	0.98[ASN][1000 genomes]
rs2370884	0.89[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs4672568	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62203001	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62203003	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62203006	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6721507	0.98[ASN][1000 genomes]
rs6725084	0.96[ASN][1000 genomes]
rs6734950	0.97[ASN][1000 genomes]
rs6735154	0.87[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs6736750	0.98[ASN][1000 genomes]
rs6739786	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6753282	0.84[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7556821	0.94[ASN][1000 genomes]
rs7558394	0.98[ASN][1000 genomes]
rs7582804	0.98[ASN][1000 genomes]
rs7583039	0.98[ASN][1000 genomes]
rs7592060	0.99[ASN][1000 genomes]
rs7596691	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs867342	0.98[ASN][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	esv1802749	chr2:210905194-211255611	Strong transcription ZNF genes & repeats Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	esv1803710	chr2:211073376-211173763	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1012567	chr2:211087588-211315554	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv834520	chr2:211101265-211257068	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv875767	chr2:211119233-211334647	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv1014508	chr2:211142855-211215068	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1010916	chr2:211147730-211205281	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211163400-211167400	Active TSS	Fetal Muscle Leg	muscle
2	chr2:211163400-211168600	Active TSS	Skeletal Muscle Male	skeletal muscle
3	chr2:211163400-211168800	Active TSS	Skeletal Muscle Female	skeletal muscle
4	chr2:211164600-211168800	Active TSS	Fetal Muscle Trunk	muscle
5	chr2:211166400-211174000	Weak transcription	Psoas Muscle	Psoas
6	chr2:211166600-211168600	Enhancers	HSMM	muscle
7	chr2:211167000-211167600	Flanking Active TSS	HSMMtube	muscle
8	chr2:211167000-211168000	Enhancers	NH-A	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links