Variant report

Variant	rs2497814
Chromosome Location	chr10:18363924-18363925
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12255303	0.83[EUR][1000 genomes]
rs2488152	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2488156	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2488157	0.94[ASN][1000 genomes]
rs2488159	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2497800	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2497804	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2497808	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2497809	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2497810	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2497812	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2497813	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2497818	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2497819	0.94[ASN][1000 genomes]
rs2497822	0.89[EUR][1000 genomes];0.94[ASN][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	nsv550039	chr10:18363924-18425519	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	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	chr10:18363000-18368000	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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