Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10131119	0.96[ASN][1000 genomes]
rs10137751	0.91[ASN][1000 genomes]
rs10144027	1.00[ASN][1000 genomes]
rs10146714	1.00[ASN][1000 genomes]
rs10483755	1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1387756	1.00[ASN][1000 genomes]
rs17100280	1.00[EUR][1000 genomes]
rs17100353	0.82[ASN][1000 genomes]
rs2101552	0.98[ASN][1000 genomes]
rs2130445	0.98[ASN][1000 genomes]
rs2171878	0.98[ASN][1000 genomes]
rs4899094	0.98[ASN][1000 genomes]
rs4902182	1.00[ASN][1000 genomes]
rs58463179	1.00[AMR][1000 genomes]
rs7141855	0.91[ASN][1000 genomes]
rs7141868	0.91[ASN][1000 genomes]
rs7154700	0.98[ASN][1000 genomes]
rs7157416	0.95[ASN][1000 genomes]
rs7157560	0.91[ASN][1000 genomes]
rs73271163	0.87[ASN][1000 genomes]
rs73271176	0.87[ASN][1000 genomes]
rs73271181	0.85[ASN][1000 genomes]
rs73271182	0.89[ASN][1000 genomes]
rs73271187	0.87[ASN][1000 genomes]
rs73271188	0.87[ASN][1000 genomes]
rs73271190	0.85[ASN][1000 genomes]
rs73271194	0.87[ASN][1000 genomes]
rs74058950	1.00[ASN][1000 genomes]
rs8003765	0.80[ASN][1000 genomes]
rs8010787	0.85[ASN][1000 genomes]
rs8010814	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[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	nsv527675	chr14:63168547-63211280	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63178600-63193000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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