Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10169075	1.00[AFR][1000 genomes]
rs10170747	1.00[AFR][1000 genomes]
rs12987628	1.00[AFR][1000 genomes]
rs1401837	1.00[AFR][1000 genomes]
rs1404085	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404088	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1405339	1.00[AFR][1000 genomes]
rs1405341	1.00[AFR][1000 genomes]
rs1526642	1.00[AFR][1000 genomes]
rs1526648	1.00[AFR][1000 genomes]
rs1533985	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1554617	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1609009	1.00[AFR][1000 genomes]
rs1660568	1.00[AFR][1000 genomes]
rs1949923	1.00[AFR][1000 genomes]
rs2901743	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs391688	1.00[AFR][1000 genomes]
rs393801	1.00[AFR][1000 genomes]
rs414148	1.00[AFR][1000 genomes]
rs7576329	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7589273	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834265	chr2:76275611-76450728	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv999645	chr2:76317006-76451354	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv874311	chr2:76389455-76492999	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 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	chr2:76419000-76419800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:76419200-76420800	Enhancers	HepG2	liver

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