Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10133646	0.85[CHB][hapmap];0.89[JPT][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10142438	0.86[ASN][1000 genomes]
rs10142615	0.86[ASN][1000 genomes]
rs1022855	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10431621	0.80[ASN][1000 genomes]
rs11625940	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11846415	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs11848944	0.85[ASN][1000 genomes]
rs17112380	0.85[ASN][1000 genomes]
rs17112395	0.80[AMR][1000 genomes]
rs1957869	0.85[ASN][1000 genomes]
rs1957874	0.81[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2181736	0.87[ASN][1000 genomes]
rs2209228	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2224838	0.83[ASN][1000 genomes]
rs4904978	0.83[ASN][1000 genomes]
rs6572117	0.84[ASN][1000 genomes]
rs721222	0.83[ASN][1000 genomes]
rs7359052	0.85[JPT][hapmap]
rs737003	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs8020905	0.86[ASN][1000 genomes]
rs8022872	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs988740	0.86[ASN][1000 genomes]
rs988741	0.87[ASN][1000 genomes]
rs988805	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	nsv901740	chr14:42386859-42477256	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42454000-42455200	Weak transcription	Primary B cells from cord blood	blood

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