Variant report

Variant	rs3891382
Chromosome Location	chr10:23559472-23559473
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10741026	0.81[AMR][1000 genomes]
rs10764397	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10764398	0.81[CHB][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10828415	0.87[CHB][hapmap];0.81[JPT][hapmap];0.89[AMR][1000 genomes]
rs10828419	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10828421	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10828422	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10828423	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10828425	0.86[JPT][hapmap]
rs10828430	0.85[AMR][1000 genomes]
rs10828431	0.85[AMR][1000 genomes]
rs11013356	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11013364	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11013369	0.91[JPT][hapmap]
rs11013376	0.88[YRI][hapmap];0.81[AFR][1000 genomes]
rs11013378	0.86[JPT][hapmap]
rs11013386	0.81[ASN][1000 genomes]
rs11013397	0.85[AMR][1000 genomes]
rs11013404	0.85[AMR][1000 genomes]
rs11013412	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11813971	0.87[ASN][1000 genomes]
rs12217944	0.86[JPT][hapmap]
rs12246990	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12248355	0.83[AFR][1000 genomes]
rs12266732	0.87[YRI][hapmap];0.81[AFR][1000 genomes]
rs12569400	0.86[JPT][hapmap]
rs12571348	0.98[ASN][1000 genomes]
rs4144623	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4258280	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4359107	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4378291	0.85[AFR][1000 genomes]
rs4382803	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4433485	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4454613	0.94[CHB][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs4528217	0.85[AFR][1000 genomes]
rs4587637	0.86[JPT][hapmap]
rs4626975	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4747453	0.89[AMR][1000 genomes]
rs4747455	0.96[YRI][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4747460	0.86[JPT][hapmap]
rs4747461	0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs4747466	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4748844	0.87[CHB][hapmap];0.86[JPT][hapmap];0.84[AMR][1000 genomes]
rs4748850	1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4748860	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs4748861	0.82[JPT][hapmap]
rs4748866	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4748877	0.82[AMR][1000 genomes]
rs61629455	0.82[AMR][1000 genomes]
rs7907909	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7919530	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831810	chr10:23445647-23605270	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv466834	chr10:23482635-23623523	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv550213	chr10:23482635-23623523	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island 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	chr10:23555600-23564200	Weak transcription	Pancreas	Pancrea

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