Variant report

Variant	rs34685815
Chromosome Location	chr9:84755772-84755773
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11139500	0.84[ASN][1000 genomes]
rs1327253	0.92[ASN][1000 genomes]
rs2767713	0.82[ASN][1000 genomes]
rs2767714	0.82[ASN][1000 genomes]
rs2767715	0.82[ASN][1000 genomes]
rs2767716	0.82[ASN][1000 genomes]
rs2767719	0.86[ASN][1000 genomes]
rs2788116	0.83[ASN][1000 genomes]
rs2788117	0.86[ASN][1000 genomes]
rs4442221	0.91[ASN][1000 genomes]
rs4877686	0.92[ASN][1000 genomes]
rs7853615	0.92[ASN][1000 genomes]
rs7853639	0.92[ASN][1000 genomes]
rs995173	0.87[ASN][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	nsv1049305	chr9:84667596-84918690	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv831640	chr9:84695958-84880535	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr9:84754800-84755800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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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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