Variant report

Variant	rs73974608
Chromosome Location	chr2:181710764-181710765
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10183078	1.00[ASN][1000 genomes]
rs11892044	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11899268	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13035717	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13392009	0.98[ASN][1000 genomes]
rs13420158	0.98[ASN][1000 genomes]
rs55689047	0.98[ASN][1000 genomes]
rs57387041	0.95[ASN][1000 genomes]
rs57416358	0.98[ASN][1000 genomes]
rs6740504	0.82[EUR][1000 genomes]
rs73974605	1.00[ASN][1000 genomes]
rs7609144	0.84[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	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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:181707800-181710800	Weak transcription	Fetal Brain Female	brain
2	chr2:181710600-181710800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:181710600-181710800	Enhancers	Fetal Lung	lung

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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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