Variant report

Variant	rs1121705
Chromosome Location	chr12:62397555-62397556
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10506434	0.86[ASN][1000 genomes]
rs10877781	1.00[JPT][hapmap]
rs11174271	0.90[ASN][1000 genomes]
rs11174276	0.80[YRI][hapmap]
rs11174279	1.00[JPT][hapmap]
rs1156947	1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs11835677	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs11836487	0.84[ASN][1000 genomes]
rs12831463	0.84[ASN][1000 genomes]
rs1371918	1.00[JPT][hapmap]
rs1373454	0.84[ASN][1000 genomes]
rs1440723	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1440724	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1561629	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17125609	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17125631	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17654373	0.84[ASN][1000 genomes]
rs17704825	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17705406	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1838380	1.00[JPT][hapmap]
rs34008431	0.84[ASN][1000 genomes]
rs4965015	1.00[JPT][hapmap]
rs56085119	0.86[ASN][1000 genomes]
rs56279780	0.84[ASN][1000 genomes]
rs7314952	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73314023	0.86[ASN][1000 genomes]
rs9668399	0.84[ASN][1000 genomes]
rs9668407	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs9668420	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs9668428	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs9669003	0.84[ASN][1000 genomes]
rs9669020	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs9669149	1.00[JPT][hapmap]
rs9669351	0.84[ASN][1000 genomes]
rs9669481	0.81[ASN][1000 genomes]
rs9669783	0.84[ASN][1000 genomes]
rs9669794	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs9737644	1.00[JPT][hapmap]
rs9739051	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs9739059	0.84[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	nsv1039741	chr12:62046850-62491052	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62396600-62398400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr12:62396800-62397600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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