Variant report

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

rs_ID	r²[population]
rs10493513	0.81[AMR][1000 genomes]
rs11210084	0.82[EUR][1000 genomes]
rs11210085	0.82[EUR][1000 genomes]
rs12117582	0.80[EUR][1000 genomes]
rs12129026	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12129942	0.87[EUR][1000 genomes]
rs12136682	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12724056	0.82[AMR][1000 genomes]
rs12745861	0.82[AMR][1000 genomes]
rs1464952	0.82[EUR][1000 genomes]
rs1525978	0.87[EUR][1000 genomes]
rs1525979	0.87[EUR][1000 genomes]
rs1917881	0.87[EUR][1000 genomes]
rs2841192	0.88[EUR][1000 genomes]
rs2901713	0.87[EUR][1000 genomes]
rs61774086	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6682845	0.82[AMR][1000 genomes]
rs6689491	0.82[EUR][1000 genomes]
rs7546928	0.88[EUR][1000 genomes]
rs940917	0.88[EUR][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	nsv1013549	chr1:73209040-73408373	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1001105	chr1:73262558-73319499	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:73304400-73309600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:73304400-73312400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:73304400-73312800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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