Variant report

Variant	rs9826923
Chromosome Location	chr3:94703331-94703332
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11918924	1.00[AMR][1000 genomes]
rs1374902	1.00[AMR][1000 genomes]
rs300302	1.00[AMR][1000 genomes]
rs3933973	1.00[AMR][1000 genomes]
rs4274746	1.00[AMR][1000 genomes]
rs4337639	1.00[AMR][1000 genomes]
rs4510376	1.00[AMR][1000 genomes]
rs4588362	1.00[AMR][1000 genomes]
rs4642127	1.00[AMR][1000 genomes]
rs4857472	1.00[AMR][1000 genomes]
rs7610104	1.00[AMR][1000 genomes]
rs7610499	1.00[AMR][1000 genomes]
rs7635917	1.00[AMR][1000 genomes]
rs9878411	1.00[AMR][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	nsv877169	chr3:94675697-94840854	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region 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	chr3:94703000-94703400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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