Variant report

Variant	rs34007569
Chromosome Location	chr2:116318580-116318581
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:11)

rs_ID	r²[population]
rs11687863	0.89[ASN][1000 genomes]
rs12618777	0.82[ASN][1000 genomes]
rs12990349	0.86[ASN][1000 genomes]
rs12993265	0.82[ASN][1000 genomes]
rs12997176	0.86[ASN][1000 genomes]
rs1839142	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34425688	0.83[EUR][1000 genomes]
rs6542278	0.87[EUR][1000 genomes]
rs6738624	0.84[ASN][1000 genomes]
rs6741692	0.82[ASN][1000 genomes]
rs6744736	0.95[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	nsv1014859	chr2:116196951-116938584	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:116318400-116318600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:116318400-116322000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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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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