Variant report

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs17697043	1.00[AFR][1000 genomes]
rs35215901	1.00[AFR][1000 genomes];0.96[EUR][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	nsv1382	chr14:84487547-84532237	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	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	chr14:84489800-84493800	Weak transcription	Fetal Stomach	stomach
2	chr14:84491000-84493200	Weak transcription	Ovary	ovary
3	chr14:84492200-84495400	Weak transcription	Fetal Lung	lung

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