Variant report

Variant	rs6083631
Chromosome Location	chr20:24800992-24800993
allele	C/G
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:79)

rs_ID	r²[population]
rs1029031	0.80[EUR][1000 genomes]
rs1029033	0.80[EUR][1000 genomes]
rs1113872	0.84[EUR][1000 genomes]
rs1122607	0.92[EUR][1000 genomes]
rs11697463	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11700139	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11700161	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11905160	0.82[EUR][1000 genomes]
rs1331285	0.84[EUR][1000 genomes]
rs1331290	0.84[EUR][1000 genomes]
rs1411892	0.83[EUR][1000 genomes]
rs1411894	0.83[EUR][1000 genomes]
rs1411895	0.83[EUR][1000 genomes]
rs1413069	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1571772	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1831483	0.83[EUR][1000 genomes]
rs1888655	0.89[EUR][1000 genomes]
rs2064404	1.00[CHB][hapmap]
rs4239751	1.00[CHB][hapmap]
rs4815358	1.00[CHB][hapmap]
rs4815359	1.00[CHB][hapmap]
rs55702326	0.81[EUR][1000 genomes]
rs55905952	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55979003	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56000345	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6036915	0.93[EUR][1000 genomes]
rs6036943	0.88[EUR][1000 genomes]
rs6036946	0.88[EUR][1000 genomes]
rs6036951	0.84[EUR][1000 genomes]
rs6036955	0.83[EUR][1000 genomes]
rs6036971	0.80[EUR][1000 genomes]
rs6036972	0.80[EUR][1000 genomes]
rs6049996	0.87[EUR][1000 genomes]
rs6050000	0.93[EUR][1000 genomes]
rs6050002	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6050007	0.90[EUR][1000 genomes]
rs6050051	0.85[EUR][1000 genomes]
rs6050058	0.88[EUR][1000 genomes]
rs6050070	0.84[EUR][1000 genomes]
rs6050073	0.84[EUR][1000 genomes]
rs6050074	0.84[EUR][1000 genomes]
rs6050114	0.80[EUR][1000 genomes]
rs6050115	0.80[EUR][1000 genomes]
rs6050116	0.80[EUR][1000 genomes]
rs6076279	0.86[EUR][1000 genomes]
rs6076281	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6076283	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6076290	0.88[EUR][1000 genomes]
rs6076292	0.86[EUR][1000 genomes]
rs6083628	0.89[EUR][1000 genomes]
rs6083630	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6083632	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6083633	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6083652	0.84[EUR][1000 genomes]
rs6083656	0.84[EUR][1000 genomes]
rs6083658	0.84[EUR][1000 genomes]
rs6083697	1.00[CHB][hapmap]
rs6083714	1.00[CHB][hapmap]
rs6106968	0.80[EUR][1000 genomes]
rs6114921	0.80[EUR][1000 genomes]
rs62215817	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62215819	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62215820	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62215821	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62215822	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62215823	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62215824	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62215826	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62215832	0.85[EUR][1000 genomes]
rs6515538	0.89[EUR][1000 genomes]
rs7262604	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7269852	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73101427	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73337207	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7509561	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs761368	1.00[CHB][hapmap]
rs765834	1.00[CHB][hapmap]
rs8117102	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs8117164	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3332519	chr20:24535099-24815615	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1061412	chr20:24629468-24887869	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv544216	chr20:24629468-24887869	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1061281	chr20:24711635-24815107	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv544217	chr20:24711635-24815107	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv912825	chr20:24715544-24813345	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv1061455	chr20:24733120-24861801	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv544218	chr20:24733120-24861801	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 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	chr20:24794200-24817600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links