Variant report

Variant	rs863394
Chromosome Location	chr12:86594783-86594784
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10745407	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs10745408	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs10776953	0.91[EUR][1000 genomes]
rs10776955	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs10776961	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs10858408	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs10858412	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs12582690	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs1493408	0.90[EUR][1000 genomes]
rs1493415	0.87[CHB][hapmap];0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs1493420	0.90[EUR][1000 genomes]
rs1493421	0.84[EUR][1000 genomes]
rs1602848	0.98[ASN][1000 genomes]
rs1628799	0.86[CHB][hapmap]
rs1689357	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1698787	1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[ASN][1000 genomes]
rs17013664	0.93[CHB][hapmap]
rs17013683	0.86[CHB][hapmap]
rs1948448	0.87[ASN][1000 genomes]
rs1986603	0.80[CHB][hapmap]
rs1994863	0.91[CHB][hapmap];0.81[ASN][1000 genomes]
rs2220782	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs2250915	0.90[EUR][1000 genomes]
rs2405925	0.82[JPT][hapmap]
rs2405928	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs2405930	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs2406115	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs2406116	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs2406118	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs2406122	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs2406123	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs2406127	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs2406128	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs2452807	0.87[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs2465143	0.87[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs2465144	0.87[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs2465147	0.87[ASN][1000 genomes]
rs2471560	1.00[CHB][hapmap];0.94[JPT][hapmap];0.99[ASN][1000 genomes]
rs2471561	0.85[EUR][1000 genomes]
rs2471562	0.91[EUR][1000 genomes]
rs2471563	0.85[EUR][1000 genomes]
rs2471568	0.87[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs2471569	0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs2471570	0.87[ASN][1000 genomes]
rs2897280	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs4265650	0.86[CHB][hapmap];0.88[JPT][hapmap]
rs4628748	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs6538023	0.89[CHB][hapmap];0.80[ASN][1000 genomes]
rs6538024	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6538025	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs6538029	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs6538033	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs7135177	0.87[CHB][hapmap];0.93[JPT][hapmap]
rs7299319	0.81[JPT][hapmap]
rs7953196	0.86[CHB][hapmap];0.94[JPT][hapmap]
rs7957560	0.87[CHB][hapmap];0.88[JPT][hapmap]
rs7964553	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs7972484	0.87[CHB][hapmap];0.87[JPT][hapmap]
rs7973773	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs839101	0.97[ASN][1000 genomes]
rs839104	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs839105	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs839118	0.86[CHB][hapmap]
rs839136	0.87[CHB][hapmap]
rs839137	0.93[CHB][hapmap]
rs839148	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs839149	1.00[CHB][hapmap];0.94[JPT][hapmap];0.81[YRI][hapmap]
rs839150	0.91[CHB][hapmap];0.93[JPT][hapmap]
rs839151	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs839152	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs839153	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs839154	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs839156	1.00[CHB][hapmap];0.94[JPT][hapmap];0.89[YRI][hapmap]
rs839157	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs839158	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs839159	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs839163	0.86[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs839164	0.86[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs839165	1.00[CHB][hapmap];0.94[JPT][hapmap];0.98[ASN][1000 genomes]
rs839166	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs839168	1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[ASN][1000 genomes]
rs839170	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs839171	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs844434	1.00[CHB][hapmap];0.94[JPT][hapmap];0.85[YRI][hapmap]
rs844435	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs863392	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs863395	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs865138	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs865721	1.00[CHB][hapmap];0.94[JPT][hapmap]

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	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	esv3442004	chr12:86514695-86599965	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	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
7	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
8	nsv800	chr12:86572379-86617887	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86594200-86594800	Enhancers	Dnd41	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links