Variant report

Variant	rs9527179
Chromosome Location	chr13:54727347-54727348
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs12427903	0.82[AMR][1000 genomes]
rs1334874	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1335976	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1335977	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1335979	0.97[EUR][1000 genomes]
rs1335980	0.95[EUR][1000 genomes]
rs1577576	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1763779	0.90[EUR][1000 genomes]
rs1932503	0.97[EUR][1000 genomes]
rs2005372	0.97[EUR][1000 genomes]
rs2050534	0.95[EUR][1000 genomes]
rs2050535	0.97[EUR][1000 genomes]
rs2050536	0.97[EUR][1000 genomes]
rs2152503	0.97[EUR][1000 genomes]
rs2184678	0.97[EUR][1000 genomes]
rs2210849	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2408992	0.95[EUR][1000 genomes]
rs2408993	0.97[EUR][1000 genomes]
rs2408994	0.97[EUR][1000 genomes]
rs2408995	0.97[EUR][1000 genomes]
rs2409027	0.82[AFR][1000 genomes]
rs2784566	0.82[AMR][1000 genomes]
rs4274311	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4883848	0.97[EUR][1000 genomes]
rs4883850	0.97[EUR][1000 genomes]
rs4884867	0.97[EUR][1000 genomes]
rs5002542	0.97[EUR][1000 genomes]
rs5002543	0.97[EUR][1000 genomes]
rs510147	0.90[EUR][1000 genomes]
rs551408	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs564930	0.93[EUR][1000 genomes]
rs574623	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs600930	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61956190	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs653228	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6561768	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs657383	0.90[EUR][1000 genomes]
rs667408	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs681704	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs706588	0.98[ASN][1000 genomes]
rs7326186	0.91[EUR][1000 genomes]
rs7326388	0.97[EUR][1000 genomes]
rs7329766	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7335075	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7335475	0.97[EUR][1000 genomes]
rs7984593	0.97[EUR][1000 genomes]
rs7985320	0.97[EUR][1000 genomes]
rs7985834	0.98[EUR][1000 genomes]
rs7986212	0.97[EUR][1000 genomes]
rs7991755	0.97[EUR][1000 genomes]
rs7992992	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8001182	0.97[EUR][1000 genomes]
rs878943	0.97[EUR][1000 genomes]
rs9536639	0.97[EUR][1000 genomes]
rs9568990	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9596914	0.81[EUR][1000 genomes]
rs988526	0.94[EUR][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	esv3375545	chr13:54517432-54908108	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1049	chr13:54684354-54728981	Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv561701	chr13:54711276-54826104	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island 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	chr13:54722600-54736200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr13:54722600-54741200	Weak transcription	HUES6 Cell Line	embryonic stem cell

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