Variant report

Variant	rs9832660
Chromosome Location	chr3:109256211-109256212
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1528901	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1609370	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1609371	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1729603	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1729608	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1729610	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1729614	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1729623	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1732173	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1732216	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1732217	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1732219	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1732220	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1732222	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1732223	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2687274	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6437855	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6437859	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6800450	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6803024	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs884245	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs884246	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs950690	0.86[AMR][1000 genomes];0.94[EUR][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	nsv949358	chr3:108681891-109268614	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv460814	chr3:109195046-109381428	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
3	nsv591268	chr3:109195046-109381428	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv470827	chr3:109195046-109433855	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9832660	NLE1	trans	lymphoblastoid	RTeQTL

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:109248200-109259200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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