Variant report

Variant	rs35353965
Chromosome Location	chr8:78091804-78091805
allele	G/T
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]
rs10100694	0.89[ASN][1000 genomes]
rs10282777	0.92[ASN][1000 genomes]
rs12541917	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12550461	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12680335	0.81[ASN][1000 genomes]
rs1377247	0.98[ASN][1000 genomes]
rs1377254	0.84[ASN][1000 genomes]
rs1452809	0.98[ASN][1000 genomes]
rs1813571	0.85[ASN][1000 genomes]
rs1982434	1.00[ASN][1000 genomes]
rs6998856	0.90[ASN][1000 genomes]
rs71509310	0.88[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	nsv891045	chr8:77998659-78477561	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr8:78091200-78092000	Enhancers	Adipose Nuclei	Adipose

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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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