Variant report

Variant	rs2731733
Chromosome Location	chr5:75344689-75344690
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs13162056	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13174796	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1393205	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1423103	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1423104	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1553310	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1910051	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2254153	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2547455	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2547456	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs258612	0.92[EUR][1000 genomes]
rs258613	0.85[EUR][1000 genomes]
rs258614	0.84[EUR][1000 genomes]
rs2731732	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2731735	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28620	0.85[EUR][1000 genomes]
rs28621	0.86[EUR][1000 genomes]
rs30191	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs30192	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs30196	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs30197	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs30199	0.83[EUR][1000 genomes]
rs30202	0.86[EUR][1000 genomes]
rs30204	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs30205	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs30206	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs30249	0.84[EUR][1000 genomes]
rs7378518	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7443455	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7443586	0.83[AMR][1000 genomes]
rs993914	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027368	chr5:74759999-75663712	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv518475	chr5:74863041-75411804	Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2731733	CTC-235G5.3	cis	Nerve Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75343200-75345400	Weak transcription	HMEC	breast

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