Variant report

Variant	rs10210124
Chromosome Location	chr2:31262903-31262904
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10164479	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10166921	0.96[CEU][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10174368	0.96[CEU][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10192472	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10197865	0.96[CEU][hapmap];0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10206704	0.85[CEU][hapmap]
rs10209881	0.96[CEU][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10210092	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10210300	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10865086	1.00[CEU][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12473730	0.92[CEU][hapmap];0.84[ASN][1000 genomes]
rs12712300	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1862964	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1862965	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1862966	0.96[CEU][hapmap];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1862967	0.96[CEU][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1862968	0.96[CEU][hapmap];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2113487	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2113488	0.96[CEU][hapmap];0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2161835	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2194454	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2194456	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2194457	0.81[ASN][1000 genomes]
rs2365191	0.85[ASN][1000 genomes]
rs4951959	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4952027	0.85[CEU][hapmap]
rs4952028	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4952030	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4952031	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4952032	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4952033	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4952038	0.86[ASN][1000 genomes]
rs5009910	0.96[CEU][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56284247	0.89[ASN][1000 genomes]
rs62140629	0.84[ASN][1000 genomes]
rs6543594	0.84[CEU][hapmap]
rs6543595	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6708989	0.95[CEU][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6752071	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6752303	0.96[CEU][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6752662	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7558425	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7565923	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7579017	0.81[CEU][hapmap]
rs7582401	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7592553	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7601904	0.85[CEU][hapmap]
rs7605643	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7608731	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9308914	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9679162	0.96[CEU][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948552	chr2:31118599-31595424	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31251400-31270000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:31260200-31265600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:31261800-31264400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr2:31262000-31272200	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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