Variant report

Variant	rs1413797
Chromosome Location	chr9:84527519-84527520
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10118455	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap]
rs10217389	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs11139464	1.00[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap]
rs11139465	1.00[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap]
rs12001732	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12338395	0.87[AMR][1000 genomes]
rs12338553	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12339026	1.00[JPT][hapmap]
rs12340419	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12341327	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12341627	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12342604	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12345231	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.88[TSI][hapmap];0.82[AMR][1000 genomes]
rs12345266	0.87[AMR][1000 genomes]
rs12351812	0.87[AMR][1000 genomes]
rs1334759	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes]
rs1334760	1.00[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap]
rs1334761	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1413798	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs1855607	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes]
rs56281129	0.87[AMR][1000 genomes]
rs57386263	0.87[AMR][1000 genomes]
rs58931877	0.87[AMR][1000 genomes]
rs60427225	0.82[AMR][1000 genomes]
rs6559647	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap]
rs6559649	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7023372	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7865884	1.00[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap]
rs9987870	0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831639	chr9:84501548-84651151	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv508555	chr9:84507699-84580028	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv1820579	chr9:84518394-84556369	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv1849322	chr9:84518394-84564267	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv1800180	chr9:84519751-84557638	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island lncRNA	4 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	chr9:84526600-84527800	Enhancers	Liver	Liver

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