Variant report

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

rs_ID	r²[population]
rs10889787	1.00[ASN][1000 genomes]
rs10889788	1.00[ASN][1000 genomes]
rs10889789	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1388654	0.97[ASN][1000 genomes]
rs1492064	1.00[ASN][1000 genomes]
rs1844937	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4625320	0.90[ASN][1000 genomes]
rs4926377	0.96[ASN][1000 genomes]
rs4926378	0.97[ASN][1000 genomes]
rs6588337	0.85[ASN][1000 genomes]
rs6656449	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6672452	0.90[ASN][1000 genomes]
rs6680906	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6694895	0.96[ASN][1000 genomes]
rs7523563	0.96[ASN][1000 genomes]
rs7527747	0.87[ASN][1000 genomes]
rs7531243	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7534385	1.00[ASN][1000 genomes]
rs854272	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9326085	0.87[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	nsv527722	chr1:69212053-69323222	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:69242800-69244000	Enhancers	Fetal Heart	heart
2	chr1:69242800-69244800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr1:69242800-69245000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:69243000-69244400	Enhancers	Rectal Smooth Muscle	rectum
5	chr1:69243000-69245200	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr1:69243200-69245000	Enhancers	Primary hematopoietic stem cells	blood

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