Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10493477	1.00[ASN][1000 genomes]
rs17131389	1.00[ASN][1000 genomes]
rs17131391	1.00[ASN][1000 genomes]
rs17131397	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17131398	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17131404	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17131405	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17131406	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17131408	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17131415	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17536833	1.00[ASN][1000 genomes]
rs1932054	1.00[ASN][1000 genomes]
rs1932055	1.00[ASN][1000 genomes]
rs1932056	1.00[ASN][1000 genomes]
rs4344268	1.00[ASN][1000 genomes]
rs61635159	1.00[ASN][1000 genomes]
rs72926249	1.00[ASN][1000 genomes]
rs72926251	1.00[ASN][1000 genomes]
rs72926259	1.00[ASN][1000 genomes]
rs72926263	1.00[ASN][1000 genomes]
rs951353	1.00[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	nsv871024	chr1:71088106-71169865	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	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	chr1:71151800-71152400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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