Variant report

Variant	rs10934013
Chromosome Location	chr3:109831059-109831060
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs12488462	0.86[ASN][1000 genomes]
rs12493551	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12637125	0.82[ASN][1000 genomes]
rs1356633	0.84[ASN][1000 genomes]
rs1381360	0.84[ASN][1000 genomes]
rs1519006	0.84[ASN][1000 genomes]
rs1519007	0.91[ASN][1000 genomes]
rs34043619	0.89[ASN][1000 genomes]
rs35134600	0.82[ASN][1000 genomes]
rs4346576	0.86[ASN][1000 genomes]
rs4682557	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4682558	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4682559	1.00[EUR][1000 genomes]
rs4682560	1.00[EUR][1000 genomes]
rs61293429	0.84[ASN][1000 genomes]
rs72937086	0.86[EUR][1000 genomes]
rs7612345	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877332	chr3:109575764-110186611	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv829667	chr3:109786662-109939671	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
3	nsv1003617	chr3:109822033-109865265	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
4	nsv3940	chr3:109825950-109870342	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:109829800-109831200	Weak transcription	Fetal Heart	heart
2	chr3:109830400-109831800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr3:109830600-109831200	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr3:109830600-109832000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr3:109830800-109831800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr3:109830800-109831800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr3:109830800-109831800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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