Variant report

Variant	rs12427865
Chromosome Location	chr13:89277710-89277711
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs12853631	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1326421	0.98[ASN][1000 genomes]
rs1326422	0.98[ASN][1000 genomes]
rs1326423	0.90[ASN][1000 genomes]
rs1326424	0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1326426	0.81[CHB][hapmap];0.82[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs1326427	0.89[ASN][1000 genomes]
rs1326428	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1326444	0.87[ASN][1000 genomes]
rs1409452	0.98[ASN][1000 genomes]
rs1409453	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1409454	0.98[ASN][1000 genomes]
rs1536352	0.81[AMR][1000 genomes]
rs1536355	0.98[ASN][1000 genomes]
rs1536356	0.89[ASN][1000 genomes]
rs1536357	0.89[ASN][1000 genomes]
rs1536358	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1853978	0.82[ASN][1000 genomes]
rs1926478	0.81[AMR][1000 genomes]
rs1952189	0.98[ASN][1000 genomes]
rs2038934	0.91[ASN][1000 genomes]
rs2038935	0.90[ASN][1000 genomes]
rs2225048	0.98[ASN][1000 genomes]
rs4310726	0.81[AMR][1000 genomes]
rs4447288	0.86[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs4519197	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4547212	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6492230	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7326991	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7330466	0.83[ASN][1000 genomes]
rs7335014	0.82[ASN][1000 genomes]
rs7335817	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7983711	0.96[ASN][1000 genomes]
rs7983924	0.98[ASN][1000 genomes]
rs7987127	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7987540	0.98[ASN][1000 genomes]
rs7993257	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8000708	0.90[ASN][1000 genomes]
rs8000777	0.98[ASN][1000 genomes]
rs8002705	0.83[ASN][1000 genomes]
rs9301420	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs9301421	0.86[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs9515129	0.98[ASN][1000 genomes]
rs9521545	0.86[ASN][1000 genomes]
rs9521558	0.98[ASN][1000 genomes]
rs9521561	0.98[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	nsv870345	chr13:89164439-89295782	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1051177	chr13:89219432-89359036	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv900816	chr13:89224649-89392881	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1051359	chr13:89258679-89311805	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89275600-89278600	Weak transcription	NHEK	skin
2	chr13:89277400-89278600	Weak transcription	Primary T helper cells PMA-I stimulated	--

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