Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10139152	1.00[ASN][1000 genomes]
rs10149999	1.00[ASN][1000 genomes]
rs10151794	1.00[ASN][1000 genomes]
rs17110868	0.83[ASN][1000 genomes]
rs55859597	1.00[ASN][1000 genomes]
rs56933416	1.00[AMR][1000 genomes]
rs57315708	0.83[ASN][1000 genomes]
rs7151041	0.83[ASN][1000 genomes]
rs73326644	1.00[AMR][1000 genomes]
rs73326672	1.00[AMR][1000 genomes]
rs73328649	1.00[AMR][1000 genomes]
rs73328655	1.00[AMR][1000 genomes]
rs73328682	1.00[AMR][1000 genomes]
rs73328690	0.83[ASN][1000 genomes]
rs73330520	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73330543	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73332696	1.00[AMR][1000 genomes]
rs73336590	1.00[AMR][1000 genomes]
rs73336597	1.00[AMR][1000 genomes]
rs73338189	1.00[AMR][1000 genomes]
rs73340517	1.00[AMR][1000 genomes]
rs73340530	1.00[AMR][1000 genomes]
rs73342506	1.00[AMR][1000 genomes]
rs73342522	1.00[AMR][1000 genomes]
rs73342549	1.00[AMR][1000 genomes]
rs73342554	1.00[AMR][1000 genomes]
rs74066058	0.83[ASN][1000 genomes]
rs74066062	1.00[EUR][1000 genomes]
rs8016841	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv565290	chr14:81085129-81230117	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81083400-81109400	Weak transcription	Dnd41	blood
2	chr14:81087400-81104200	Weak transcription	HSMM	muscle
3	chr14:81088600-81099400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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