Variant report

Variant	rs57494713
Chromosome Location	chr10:18665187-18665188
allele	A/G
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:10)

rs_ID	r²[population]
rs11013834	0.83[EUR][1000 genomes]
rs11013890	0.95[ASN][1000 genomes]
rs11013933	0.97[ASN][1000 genomes]
rs11013950	0.80[ASN][1000 genomes]
rs12254796	0.90[ASN][1000 genomes]
rs12262563	0.97[ASN][1000 genomes]
rs1325992	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16917197	0.86[AFR][1000 genomes]
rs4748453	0.84[ASN][1000 genomes]
rs61418170	0.92[AMR][1000 genomes];0.80[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	nsv1046458	chr10:18629603-18683860	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18652400-18667400	Weak transcription	Left Ventricle	heart
2	chr10:18659400-18676000	Weak transcription	Right Ventricle	heart
3	chr10:18662000-18667400	Weak transcription	Aorta	Aorta
4	chr10:18665000-18665200	Weak transcription	Fetal Heart	heart

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Input of quick search could be:

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

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