Variant report

Variant	rs1895018
Chromosome Location	chr8:113216074-113216075
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10105433	0.94[JPT][hapmap]
rs11786035	0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs11786941	0.94[JPT][hapmap]
rs12114136	0.95[ASN][1000 genomes]
rs1303762	0.82[JPT][hapmap]
rs1420849	0.93[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1420850	0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs1420851	0.93[JPT][hapmap];0.80[ASN][1000 genomes]
rs1420854	0.81[JPT][hapmap]
rs1420859	0.81[JPT][hapmap]
rs1592624	0.88[JPT][hapmap];0.80[ASN][1000 genomes]
rs1592625	0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs1833320	0.80[ASN][1000 genomes]
rs1833321	0.94[ASN][1000 genomes]
rs1895014	0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs1895015	0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs1895016	0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs2016614	0.81[JPT][hapmap]
rs2052343	0.95[ASN][1000 genomes]
rs2052345	0.95[ASN][1000 genomes]
rs2172352	0.82[JPT][hapmap]
rs2353273	0.90[ASN][1000 genomes]
rs2883277	0.97[ASN][1000 genomes]
rs4143627	0.81[JPT][hapmap]
rs4412394	0.94[ASN][1000 genomes]
rs4601350	0.82[JPT][hapmap]
rs4876278	0.95[ASN][1000 genomes]
rs4876279	0.95[ASN][1000 genomes]
rs4876450	0.95[ASN][1000 genomes]
rs4876459	0.80[ASN][1000 genomes]
rs4876460	0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs6983302	0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs7003531	0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs7016230	0.81[JPT][hapmap]
rs7018166	0.82[JPT][hapmap]
rs7816045	0.80[ASN][1000 genomes]
rs7821683	0.82[JPT][hapmap]
rs7830950	0.80[ASN][1000 genomes]
rs7835695	0.95[ASN][1000 genomes]
rs929684	0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs929685	0.81[JPT][hapmap]
rs9297467	0.80[ASN][1000 genomes]
rs950985	0.94[JPT][hapmap];0.80[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	nsv533857	chr8:112819659-113801258	Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	nsv891321	chr8:112978128-113229425	Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv891322	chr8:112978128-113267916	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1022457	chr8:113071774-113811177	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 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	chr8:113214800-113217400	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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