Variant report

Variant	rs11103930
Chromosome Location	chr12:86718908-86718909
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 120 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:108)

rs_ID	r²[population]
rs10745407	0.83[JPT][hapmap]
rs10745408	0.83[JPT][hapmap]
rs10745416	0.84[JPT][hapmap]
rs10776955	0.83[JPT][hapmap]
rs10776961	0.80[CHD][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs10858408	0.83[JPT][hapmap]
rs10858412	0.84[JPT][hapmap]
rs10858415	0.82[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.82[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap]
rs11830208	0.81[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap]
rs11830448	0.94[CHB][hapmap];0.82[GIH][hapmap];0.88[JPT][hapmap]
rs12303046	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12306280	0.88[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs12309874	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12319410	0.94[CHB][hapmap];0.86[CHD][hapmap];0.88[GIH][hapmap];0.88[JPT][hapmap];0.88[MKK][hapmap]
rs12319593	0.88[CHB][hapmap];0.86[JPT][hapmap]
rs12579580	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs12581639	0.88[CHB][hapmap];0.82[GIH][hapmap];0.88[JPT][hapmap]
rs12581912	0.94[CHB][hapmap];0.82[JPT][hapmap]
rs12582690	0.83[CHB][hapmap];0.84[JPT][hapmap]
rs12582767	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs1628799	0.88[JPT][hapmap]
rs1698787	0.83[JPT][hapmap]
rs17013664	0.88[JPT][hapmap]
rs17013683	0.88[JPT][hapmap]
rs17013858	0.94[CHB][hapmap];0.88[JPT][hapmap]
rs17013981	0.82[CHB][hapmap];0.88[JPT][hapmap]
rs17014005	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs17014008	0.88[JPT][hapmap]
rs17014009	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs17014020	0.87[CHB][hapmap];0.88[JPT][hapmap]
rs17014026	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs17040806	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs1986602	0.94[CHB][hapmap];0.88[JPT][hapmap]
rs1986603	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs1994863	0.86[JPT][hapmap]
rs2141927	0.94[CHB][hapmap];0.86[CHD][hapmap];0.88[GIH][hapmap];0.83[JPT][hapmap]
rs2220782	0.83[JPT][hapmap]
rs2405793	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs2405925	0.84[JPT][hapmap]
rs2405928	0.84[JPT][hapmap]
rs2405929	0.94[CHB][hapmap];0.86[CHD][hapmap];0.88[GIH][hapmap];0.88[JPT][hapmap]
rs2405930	0.89[JPT][hapmap];0.81[ASN][1000 genomes]
rs2405931	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2406115	0.80[CHD][hapmap];0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs2406116	0.83[JPT][hapmap]
rs2406118	0.83[JPT][hapmap]
rs2406122	0.83[JPT][hapmap]
rs2406123	0.83[JPT][hapmap]
rs2406127	0.83[JPT][hapmap]
rs2406128	0.82[JPT][hapmap]
rs2406160	0.94[JPT][hapmap]
rs2452807	0.83[JPT][hapmap]
rs2465144	0.83[JPT][hapmap]
rs2471560	0.83[JPT][hapmap]
rs2471568	0.83[JPT][hapmap]
rs2471569	0.83[JPT][hapmap]
rs2897240	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs2897274	0.94[CHB][hapmap];0.86[CHD][hapmap];0.88[GIH][hapmap];0.88[JPT][hapmap]
rs2897275	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2897277	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2897278	0.94[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2897280	0.84[JPT][hapmap]
rs4370997	0.94[JPT][hapmap]
rs4488269	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs4526834	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4628748	0.80[CHD][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs4636736	0.88[CHB][hapmap];0.88[GIH][hapmap];0.88[JPT][hapmap]
rs56293486	1.00[ASN][1000 genomes]
rs57002922	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60555693	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61014498	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6538023	0.85[JPT][hapmap]
rs6538024	0.93[JPT][hapmap]
rs6538025	0.83[JPT][hapmap]
rs6538029	0.83[JPT][hapmap]
rs6538033	0.84[JPT][hapmap]
rs7135177	0.82[JPT][hapmap]
rs7299319	0.84[JPT][hapmap]
rs7301129	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs7953196	0.82[JPT][hapmap]
rs7961251	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs7964553	0.83[JPT][hapmap]
rs7973773	0.83[JPT][hapmap]
rs7980126	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs839104	0.83[JPT][hapmap]
rs839148	0.83[JPT][hapmap]
rs839149	0.83[JPT][hapmap]
rs839151	0.83[JPT][hapmap]
rs839152	0.86[JPT][hapmap]
rs839153	0.83[JPT][hapmap]
rs839156	0.83[JPT][hapmap]
rs839157	0.83[JPT][hapmap]
rs839158	0.82[JPT][hapmap]
rs839159	0.83[JPT][hapmap]
rs839162	0.88[JPT][hapmap]
rs839165	0.83[JPT][hapmap]
rs839166	0.83[JPT][hapmap]
rs839168	0.83[JPT][hapmap]
rs839170	0.82[JPT][hapmap]
rs839171	0.83[JPT][hapmap]
rs844434	0.82[JPT][hapmap]
rs844435	0.83[JPT][hapmap]
rs863392	0.82[JPT][hapmap]
rs863395	0.83[JPT][hapmap]
rs865138	0.83[JPT][hapmap]
rs865721	0.83[JPT][hapmap]
rs9919783	0.83[ASN][1000 genomes]
rs9919793	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2761759	chr12:86415936-86747726	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv518059	chr12:86416212-86747726	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1041397	chr12:86438607-86737558	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1053087	chr12:86569126-86733418	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv541564	chr12:86569126-86733418	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1037003	chr12:86610040-86798121	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1045386	chr12:86616015-86733418	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv541565	chr12:86616015-86733418	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv802	chr12:86683758-86723684	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv1845250	chr12:86696771-86730126	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	nsv1053234	chr12:86701070-86774957	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	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