Variant report

Variant	rs73305073
Chromosome Location	chr8:106738045-106738046
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10106386	0.88[ASN][1000 genomes]
rs1025856	0.81[ASN][1000 genomes]
rs11776679	0.94[ASN][1000 genomes]
rs12541049	0.99[ASN][1000 genomes]
rs12542643	0.90[ASN][1000 genomes]
rs12545480	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12545946	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12546300	0.87[ASN][1000 genomes]
rs12547056	0.91[ASN][1000 genomes]
rs1372621	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1442326	0.91[ASN][1000 genomes]
rs1578995	0.90[ASN][1000 genomes]
rs16873601	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1992471	0.91[ASN][1000 genomes]
rs2028552	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28565020	0.97[ASN][1000 genomes]
rs3779776	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4302813	0.91[ASN][1000 genomes]
rs57566398	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58307372	0.91[ASN][1000 genomes]
rs6992301	0.97[ASN][1000 genomes]
rs73305060	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73305067	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73305069	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs753534	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs753535	0.99[AFR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs753536	0.82[ASN][1000 genomes]
rs7816793	0.97[ASN][1000 genomes]
rs7823089	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7823563	0.92[ASN][1000 genomes]
rs7836294	0.81[AFR][1000 genomes]
rs9643019	0.87[EUR][1000 genomes]
rs9643020	0.99[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021369	chr8:106493317-107243322	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv831418	chr8:106648456-106833333	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv891260	chr8:106737459-106808078	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:106729200-106742600	Weak transcription	Right Ventricle	heart
2	chr8:106734200-106743200	Weak transcription	Aorta	Aorta
3	chr8:106735400-106742200	Weak transcription	K562	blood
4	chr8:106736000-106742600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr8:106738000-106738400	Enhancers	Fetal Lung	lung
6	chr8:106738000-106739200	Enhancers	Ovary	ovary
7	chr8:106738000-106742600	Weak transcription	Adipose Nuclei	Adipose

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