Variant report

Variant	rs73974605
Chromosome Location	chr2:181707313-181707314
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10183078	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13392009	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13420158	0.98[ASN][1000 genomes]
rs55689047	0.98[ASN][1000 genomes]
rs57387041	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57416358	0.98[ASN][1000 genomes]
rs73974608	1.00[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	nsv834475	chr2:181537463-181724891	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr2:181706200-181707800	Enhancers	Fetal Brain Female	brain
2	chr2:181706800-181707600	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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