Variant report

Variant	rs11012386
Chromosome Location	chr10:18342335-18342336
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10828127	0.83[EUR][1000 genomes]
rs11012311	0.83[EUR][1000 genomes]
rs11012330	0.85[EUR][1000 genomes]
rs11012333	0.85[EUR][1000 genomes]
rs11012350	0.88[EUR][1000 genomes]
rs11012368	1.00[EUR][1000 genomes]
rs11012396	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11012397	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11012398	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12358478	0.80[EUR][1000 genomes]
rs16916787	0.85[EUR][1000 genomes]
rs67406532	0.85[EUR][1000 genomes]
rs72780045	0.95[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs72780046	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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	nsv1039655	chr10:18252931-18348954	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18331600-18348800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr10:18339600-18344600	Weak transcription	Fetal Heart	heart

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

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