Variant report

Variant	rs4851951
Chromosome Location	chr2:98848414-98848415
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10172087	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10176056	0.81[ASN][1000 genomes]
rs10181000	0.85[CHB][hapmap]
rs10190336	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10199476	0.81[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10201994	0.81[ASN][1000 genomes]
rs10202618	0.83[ASN][1000 genomes]
rs10203437	0.83[ASN][1000 genomes]
rs11124096	1.00[CHB][hapmap];0.86[JPT][hapmap];0.95[ASN][1000 genomes]
rs11124107	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11124119	0.89[ASN][1000 genomes]
rs11124121	0.94[ASN][1000 genomes]
rs11673807	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11679920	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11889349	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs11891512	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11895654	1.00[CHB][hapmap];0.86[JPT][hapmap];0.95[ASN][1000 genomes]
rs11901562	0.89[ASN][1000 genomes]
rs12478763	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs12478769	0.99[ASN][1000 genomes]
rs12622324	0.81[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12624294	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12712256	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12993718	0.99[ASN][1000 genomes]
rs12993818	0.95[ASN][1000 genomes]
rs12999985	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13013876	0.99[ASN][1000 genomes]
rs13014142	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13033263	0.99[ASN][1000 genomes]
rs13394706	0.85[CHB][hapmap]
rs13408372	0.83[CHB][hapmap]
rs13415414	0.81[ASN][1000 genomes]
rs1451251	0.81[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1466944	1.00[CHB][hapmap]
rs1504679	0.83[ASN][1000 genomes]
rs17427684	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17428056	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17429208	0.92[CHB][hapmap]
rs17493655	0.81[ASN][1000 genomes]
rs17493788	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1875880	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2102270	0.91[CHB][hapmap]
rs2122756	0.81[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.81[YRI][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2202387	0.93[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2221416	1.00[CHB][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs2292118	0.92[CHB][hapmap]
rs2292119	1.00[CHB][hapmap]
rs4374424	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4389366	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4455212	1.00[CHB][hapmap];0.81[JPT][hapmap];0.93[ASN][1000 genomes]
rs4477970	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4479470	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4494805	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4535095	0.93[ASN][1000 genomes]
rs4608580	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs4632400	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4851122	0.89[ASN][1000 genomes]
rs4851123	0.83[ASN][1000 genomes]
rs4851935	1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs4851952	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4851954	0.87[ASN][1000 genomes]
rs4851955	0.83[ASN][1000 genomes]
rs62157914	0.81[ASN][1000 genomes]
rs6543419	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs6543459	0.81[ASN][1000 genomes]
rs66464436	0.81[ASN][1000 genomes]
rs6715989	1.00[CHB][hapmap];0.92[JPT][hapmap];0.81[ASN][1000 genomes]
rs6725543	0.93[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6743279	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6747344	1.00[CHB][hapmap];0.88[JPT][hapmap];0.95[ASN][1000 genomes]
rs6747410	0.92[CHB][hapmap]
rs6752440	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6754222	0.85[CHB][hapmap]
rs72933220	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72950941	0.82[ASN][1000 genomes]
rs7572757	0.81[ASN][1000 genomes]
rs7574218	0.99[ASN][1000 genomes]
rs7578802	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7589018	0.81[ASN][1000 genomes]
rs7598554	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7601049	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7601503	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7606220	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs937726	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv518056	chr2:98586842-99156296	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1004082	chr2:98792256-98967681	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv535833	chr2:98792256-98967681	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv582513	chr2:98829237-98869914	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv582514	chr2:98835962-98869914	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links