Variant report

Variant	rs2393536
Chromosome Location	chr10:61289501-61289502
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12356039	0.82[EUR][1000 genomes]
rs1414629	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1619518	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1696800	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1696801	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1763885	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1853258	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2263266	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2454767	0.85[EUR][1000 genomes];0.94[ASN][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	nsv895564	chr10:61220923-61327502	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv551150	chr10:61286904-61330297	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr10:61286000-61296400	Weak transcription	Ovary	ovary

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

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