Variant report

Variant	rs2118274
Chromosome Location	chr2:142521944-142521945
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1008830	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10195141	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12474567	0.96[ASN][1000 genomes]
rs12612082	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12612242	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12616665	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12616779	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12990449	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13034371	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1567305	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1567306	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1567307	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1567308	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16847091	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1866025	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1866027	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2009269	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2009270	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2048206	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2164697	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2164699	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2890600	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34474362	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4352182	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4954923	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs972485	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834394	chr2:142430225-142593264	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv530398	chr2:142474842-142843839	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv459663	chr2:142509570-142568465	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
4	nsv583236	chr2:142509570-142568465	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
5	nsv1004379	chr2:142514657-142547597	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:142520400-142523200	Weak transcription	Dnd41	blood

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