Variant report

Variant	rs35864527
Chromosome Location	chr10:97694837-97694838
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11594853	0.80[AMR][1000 genomes]
rs11596697	0.80[AMR][1000 genomes]
rs11597564	0.80[AMR][1000 genomes]
rs11599105	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11599779	0.80[AMR][1000 genomes]
rs12761082	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12762284	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12765198	0.88[EUR][1000 genomes]
rs12775584	0.84[EUR][1000 genomes]
rs34777055	0.82[EUR][1000 genomes]
rs34963139	0.80[AMR][1000 genomes]
rs35298116	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs35968758	0.80[AMR][1000 genomes]
rs36103691	0.80[AMR][1000 genomes]
rs66527979	0.80[AMR][1000 genomes]
rs66530311	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs66706740	0.80[AMR][1000 genomes]
rs66851219	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67166869	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs67870248	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7904176	0.85[EUR][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	nsv531923	chr10:97366055-97725757	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv895906	chr10:97513362-97703650	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv895908	chr10:97544513-97724247	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97690400-97699000	Weak transcription	Brain Substantia Nigra	brain
2	chr10:97694600-97697000	Weak transcription	Fetal Stomach	stomach
3	chr10:97694600-97697600	Weak transcription	Aorta	Aorta

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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