Variant report

Variant	rs10182153
Chromosome Location	chr2:142614752-142614753
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10168519	0.91[CEU][hapmap];0.94[CHB][hapmap];0.88[EUR][1000 genomes]
rs10204177	0.94[CEU][hapmap];0.93[CHB][hapmap]
rs10205635	0.93[YRI][hapmap]
rs1160815	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12691623	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12691624	0.95[CEU][hapmap];0.94[CHB][hapmap];0.85[JPT][hapmap]
rs12992880	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12993061	0.88[CHB][hapmap]
rs13004344	0.84[JPT][hapmap]
rs13007371	0.90[CEU][hapmap];0.94[CHB][hapmap]
rs13009181	0.86[ASN][1000 genomes]
rs13016459	0.82[CHB][hapmap]
rs13018903	0.88[CHB][hapmap];0.84[JPT][hapmap];0.82[YRI][hapmap];0.87[ASN][1000 genomes]
rs13019219	0.88[CHB][hapmap];0.84[JPT][hapmap]
rs13031421	0.88[CHB][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs13031743	0.82[CHB][hapmap]
rs13385804	1.00[YRI][hapmap]
rs13430058	0.93[YRI][hapmap]
rs1369537	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1435593	0.85[CEU][hapmap]
rs16847370	0.93[YRI][hapmap]
rs16847378	0.88[CHB][hapmap];0.85[JPT][hapmap];0.89[ASN][1000 genomes]
rs16847412	0.93[YRI][hapmap]
rs1992000	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2217964	0.83[JPT][hapmap]
rs352974	0.81[EUR][1000 genomes]
rs352976	0.86[CEU][hapmap];0.80[JPT][hapmap]
rs352978	0.85[CEU][hapmap]
rs352982	0.87[CEU][hapmap]
rs352986	0.81[JPT][hapmap]
rs4662269	0.94[CEU][hapmap];0.94[CHB][hapmap]
rs4662270	0.91[CEU][hapmap];0.94[CHB][hapmap]
rs4662271	0.83[CHB][hapmap]
rs4662467	0.91[CEU][hapmap];0.94[CHB][hapmap]
rs4662468	0.83[CHB][hapmap]
rs7586153	0.93[YRI][hapmap]

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	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
2	nsv1009893	chr2:142585905-142662116	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	nsv459674	chr2:142592560-142636907	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv583237	chr2:142592560-142636907	Enhancers Flanking Active TSS Weak transcription 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	chr2:142613600-142614800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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