Variant report

Variant	rs10203924
Chromosome Location	chr2:142869300-142869301
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1001629	0.90[ASN][1000 genomes]
rs1011862	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10173643	0.91[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs10186258	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10803489	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11683745	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12472834	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13000270	0.82[ASN][1000 genomes]
rs13024219	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1349219	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1349220	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1349221	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1349222	0.89[ASN][1000 genomes]
rs1375606	0.91[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1375609	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1375614	0.81[ASN][1000 genomes]
rs1449480	0.91[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1449481	0.82[ASN][1000 genomes]
rs1449485	0.89[ASN][1000 genomes]
rs1900935	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2167053	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2290140	0.83[EUR][1000 genomes]
rs4662219	0.87[ASN][1000 genomes]
rs4662373	0.82[ASN][1000 genomes]
rs4662389	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62155598	0.89[ASN][1000 genomes]
rs6707136	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6712994	0.99[ASN][1000 genomes]
rs6744928	0.87[ASN][1000 genomes]
rs7565655	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7586417	0.87[ASN][1000 genomes]
rs7609479	0.91[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9287332	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs997123	0.84[ASN][1000 genomes]
rs9973706	0.91[AFR][1000 genomes];0.91[ASN][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	nsv997274	chr2:142760393-143599193	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv526107	chr2:142768518-142884248	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv875254	chr2:142833327-142931146	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1006247	chr2:142851056-143289465	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:142862800-142870200	Weak transcription	Brain Anterior Caudate	brain
2	chr2:142867000-142870600	Weak transcription	Brain Substantia Nigra	brain
3	chr2:142869200-142869400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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