Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs35303723	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs3901447	0.83[ASN][1000 genomes]
rs56055951	0.96[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs56291136	0.88[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs56323244	0.97[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs57980525	0.83[ASN][1000 genomes]
rs6922956	0.83[ASN][1000 genomes]
rs6935624	0.83[ASN][1000 genomes]
rs6936142	0.83[ASN][1000 genomes]
rs73785028	0.83[ASN][1000 genomes]
rs9484976	0.99[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs9484977	0.90[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs9484978	0.93[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs9484979	0.99[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs9484980	0.99[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs9484981	0.99[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs9484984	0.83[ASN][1000 genomes]
rs9484985	0.83[ASN][1000 genomes]
rs9497276	0.93[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs9497277	0.99[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs9497278	0.97[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs9497281	0.81[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs9497282	0.81[AFR][1000 genomes];0.83[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	nsv1017166	chr6:145677071-145808448	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	1 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	chr6:145688400-145692800	Weak transcription	GM12878-XiMat	blood
2	chr6:145688600-145689600	Enhancers	Fetal Brain Male	brain

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