Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10137798	0.85[CEU][hapmap]
rs10140285	0.85[CEU][hapmap]
rs10150127	1.00[CEU][hapmap]
rs11158463	0.85[CEU][hapmap]
rs1255501	1.00[ASN][1000 genomes]
rs1255502	1.00[ASN][1000 genomes]
rs1268641	1.00[ASN][1000 genomes]
rs1950571	0.85[CEU][hapmap]
rs1956025	0.84[CEU][hapmap]
rs2355743	0.88[CEU][hapmap]
rs2356097	0.84[CEU][hapmap]
rs2749405	1.00[ASN][1000 genomes]
rs4426276	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4899101	0.88[CEU][hapmap]
rs61000383	1.00[ASN][1000 genomes]
rs6420893	0.88[CEU][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6573464	0.92[CEU][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7143072	0.85[CEU][hapmap]
rs7157658	0.89[CEU][hapmap]
rs8018884	0.84[CEU][hapmap]

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	nsv1042953	chr14:63314591-63384260	Enhancers Weak transcription	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	chr14:63364000-63369200	Weak transcription	H1 Cell Line	embryonic stem cell

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