Variant report

Variant	rs73702770
Chromosome Location	chr8:110108073-110108074
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11986646	0.86[EUR][1000 genomes]
rs11995096	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16879035	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4129683	0.86[EUR][1000 genomes]
rs61335240	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6469232	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73309523	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73311368	0.86[EUR][1000 genomes]
rs7829028	0.86[EUR][1000 genomes]
rs7839820	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022273	chr8:110026712-110146600	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv539715	chr8:110026712-110146600	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr8:110107600-110108800	Enhancers	Fetal Kidney	kidney

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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