Variant report

Variant	rs12775601
Chromosome Location	chr10:54106060-54106061
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10508971	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11001698	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11001726	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11001728	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11001729	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11812118	0.90[EUR][1000 genomes]
rs11815399	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12767827	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12776422	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12778940	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12780421	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1528873	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1528874	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1863730	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35962022	0.82[EUR][1000 genomes]
rs7908091	0.91[EUR][1000 genomes];0.97[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	nsv532194	chr10:53746620-54735550	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv895399	chr10:53900872-54219820	Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54098800-54111200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr10:54103800-54111000	Weak transcription	Osteobl	bone
3	chr10:54103800-54113600	Weak transcription	A549	lung
4	chr10:54104000-54111200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

Quick Search:

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

what's new

Quick links