Variant report

Variant	rs10438561
Chromosome Location	chr16:71470629-71470630
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs13333851	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13336790	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13339307	1.00[AMR][1000 genomes]
rs13339390	1.00[AMR][1000 genomes]
rs28620690	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs28709366	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9923065	0.83[AMR][1000 genomes]
rs9927819	0.82[AFR][1000 genomes]
rs9930279	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9930642	0.90[AFR][1000 genomes]
rs9933647	0.84[AFR][1000 genomes];1.00[AMR][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	nsv949461	chr16:71196153-71579711	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv1064435	chr16:71440719-71488771	Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71470600-71472600	Enhancers	Placenta	Placenta

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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