Variant report

Variant	rs9598199
Chromosome Location	chr13:61498109-61498110
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1067969	1.00[ASN][1000 genomes]
rs1068735	1.00[ASN][1000 genomes]
rs12428173	1.00[ASN][1000 genomes]
rs1394318	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1606637	1.00[ASN][1000 genomes]
rs17059106	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17059118	0.86[ASN][1000 genomes]
rs1847506	1.00[ASN][1000 genomes]
rs1849688	1.00[ASN][1000 genomes]
rs186181	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs186182	1.00[ASN][1000 genomes]
rs1875849	0.86[ASN][1000 genomes]
rs2655710	1.00[ASN][1000 genomes]
rs2671284	1.00[ASN][1000 genomes]
rs2770917	1.00[ASN][1000 genomes]
rs300324	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs301634	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs301686	1.00[ASN][1000 genomes]
rs301693	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3119874	0.86[ASN][1000 genomes]
rs3119876	1.00[ASN][1000 genomes]
rs3127055	1.00[ASN][1000 genomes]
rs3850087	1.00[ASN][1000 genomes]
rs3861175	1.00[ASN][1000 genomes]
rs3914416	1.00[ASN][1000 genomes]
rs3914417	1.00[ASN][1000 genomes]
rs4542547	1.00[ASN][1000 genomes]
rs4886288	0.86[CEU][hapmap]
rs4886290	0.93[CEU][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7997129	1.00[ASN][1000 genomes]
rs7998134	1.00[ASN][1000 genomes]
rs9563846	1.00[ASN][1000 genomes]
rs9570380	1.00[ASN][1000 genomes]
rs9570382	0.87[ASN][1000 genomes]
rs9598176	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9598193	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9598206	0.86[ASN][1000 genomes]
rs997706	0.87[ASN][1000 genomes]
rs997707	0.87[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832624	chr13:61383648-61553974	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island lncRNA	2 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	chr13:61497400-61498600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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