Variant report

Variant	rs6753503
Chromosome Location	chr2:37736167-37736168
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10198396	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10199137	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10204024	0.91[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap];0.90[ASN][1000 genomes]
rs10865125	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11124586	0.88[ASN][1000 genomes]
rs1113496	0.91[ASN][1000 genomes]
rs11684461	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12151464	0.87[ASN][1000 genomes]
rs13000102	0.87[ASN][1000 genomes]
rs13009200	0.81[ASN][1000 genomes]
rs13387905	0.87[ASN][1000 genomes]
rs13412538	0.87[ASN][1000 genomes]
rs17020823	0.85[ASN][1000 genomes]
rs17020835	0.87[ASN][1000 genomes]
rs2080387	0.87[ASN][1000 genomes]
rs2192942	0.89[ASN][1000 genomes]
rs2192943	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2192944	0.88[ASN][1000 genomes]
rs2216117	0.87[ASN][1000 genomes]
rs2373108	0.83[ASN][1000 genomes]
rs2373109	0.86[ASN][1000 genomes]
rs2373110	0.87[ASN][1000 genomes]
rs4353628	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4450582	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4503968	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4517954	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4670205	0.97[ASN][1000 genomes]
rs58694726	0.86[ASN][1000 genomes]
rs60691585	0.81[ASN][1000 genomes]
rs62135566	0.87[ASN][1000 genomes]
rs62135567	0.87[ASN][1000 genomes]
rs62135568	0.87[ASN][1000 genomes]
rs6544088	0.87[ASN][1000 genomes]
rs6708411	0.87[ASN][1000 genomes]
rs6724538	0.87[ASN][1000 genomes]
rs6735123	0.99[ASN][1000 genomes]
rs6746868	0.88[ASN][1000 genomes]
rs6757678	0.87[ASN][1000 genomes]
rs7557408	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7561053	0.97[ASN][1000 genomes]
rs7571760	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7574012	0.88[ASN][1000 genomes]
rs7582204	0.88[ASN][1000 genomes]
rs7588494	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7593333	0.86[ASN][1000 genomes]
rs7595792	0.87[ASN][1000 genomes]
rs960902	0.89[ASN][1000 genomes]
rs9941697	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833814	chr2:37643132-37840247	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv456374	chr2:37669487-37868214	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv470453	chr2:37669487-37868214	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv581473	chr2:37669487-37868214	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37709600-37738000	Weak transcription	Liver	Liver
2	chr2:37734600-37736400	Enhancers	Fetal Heart	heart
3	chr2:37735600-37742800	Weak transcription	Rectal Smooth Muscle	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links