Variant report

Variant	rs2061735
Chromosome Location	chr3:162253383-162253384
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10084695	1.00[ASN][1000 genomes]
rs1026691	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1026693	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10460867	1.00[ASN][1000 genomes]
rs10936280	1.00[ASN][1000 genomes]
rs10936281	1.00[ASN][1000 genomes]
rs10936283	1.00[ASN][1000 genomes]
rs11712285	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11927487	1.00[ASN][1000 genomes]
rs12696149	0.87[ASN][1000 genomes]
rs1382204	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1471415	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1478142	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1478145	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1478147	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2199604	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2318455	0.82[EUR][1000 genomes]
rs2405505	1.00[ASN][1000 genomes]
rs2405506	1.00[ASN][1000 genomes]
rs2405753	0.87[ASN][1000 genomes]
rs2405754	0.87[ASN][1000 genomes]
rs28567923	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28667121	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2897152	1.00[ASN][1000 genomes]
rs3853161	1.00[ASN][1000 genomes]
rs3863256	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3907216	1.00[ASN][1000 genomes]
rs4296607	1.00[ASN][1000 genomes]
rs4296608	1.00[ASN][1000 genomes]
rs4296609	1.00[ASN][1000 genomes]
rs4621344	1.00[ASN][1000 genomes]
rs4856629	1.00[ASN][1000 genomes]
rs4856630	1.00[ASN][1000 genomes]
rs4856631	1.00[ASN][1000 genomes]
rs4856632	1.00[ASN][1000 genomes]
rs4856633	1.00[ASN][1000 genomes]
rs4856682	0.87[ASN][1000 genomes]
rs6441452	0.87[ASN][1000 genomes]
rs6441454	0.87[ASN][1000 genomes]
rs6441459	1.00[ASN][1000 genomes]
rs6441460	1.00[ASN][1000 genomes]
rs6441461	1.00[ASN][1000 genomes]
rs6441462	1.00[ASN][1000 genomes]
rs6441463	1.00[ASN][1000 genomes]
rs6764843	1.00[ASN][1000 genomes]
rs6765996	1.00[ASN][1000 genomes]
rs6766883	1.00[ASN][1000 genomes]
rs6766973	1.00[ASN][1000 genomes]
rs6770434	1.00[ASN][1000 genomes]
rs6775708	0.87[ASN][1000 genomes]
rs6776864	1.00[ASN][1000 genomes]
rs6776986	1.00[ASN][1000 genomes]
rs6777189	1.00[ASN][1000 genomes]
rs6789202	1.00[ASN][1000 genomes]
rs6791605	1.00[ASN][1000 genomes]
rs6798305	1.00[ASN][1000 genomes]
rs6799150	1.00[ASN][1000 genomes]
rs6801086	1.00[ASN][1000 genomes]
rs6801492	1.00[ASN][1000 genomes]
rs6801686	1.00[ASN][1000 genomes]
rs7633312	1.00[ASN][1000 genomes]
rs7648533	0.87[ASN][1000 genomes]
rs9290119	1.00[ASN][1000 genomes]
rs9813453	1.00[ASN][1000 genomes]
rs9813595	1.00[ASN][1000 genomes]
rs9813898	1.00[ASN][1000 genomes]
rs9817021	1.00[ASN][1000 genomes]
rs9819929	1.00[ASN][1000 genomes]
rs9827825	0.85[EUR][1000 genomes]
rs9868667	1.00[ASN][1000 genomes]
rs9875471	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9879717	1.00[ASN][1000 genomes]
rs993391	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs993392	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877721	chr3:161878713-162303276	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1006802	chr3:161921063-162599175	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv877735	chr3:162123179-162380954	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv428424	chr3:162145988-163033943	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1012160	chr3:162182166-162540478	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1000912	chr3:162186601-162311128	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv592201	chr3:162188625-163142162	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv829775	chr3:162211618-162406402	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv470994	chr3:162217993-162945834	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv592205	chr3:162217994-162263832	Enhancers Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv877755	chr3:162218849-162386891	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv877756	chr3:162218849-162391801	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv877757	chr3:162226534-162391801	Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr3:162251200-162253400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:162251800-162257400	Weak transcription	Dnd41	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links