Variant report

Variant	rs1322063
Chromosome Location	chr9:117585482-117585483
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10759736	1.00[ASN][1000 genomes]
rs10982396	1.00[ASN][1000 genomes]
rs1322055	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs2093404	0.88[AFR][1000 genomes]
rs4246905	1.00[YRI][hapmap]
rs4372078	1.00[YRI][hapmap]
rs4978607	1.00[ASN][1000 genomes]
rs6478105	1.00[ASN][1000 genomes]
rs6478112	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7469678	1.00[ASN][1000 genomes]
rs7869598	1.00[ASN][1000 genomes]
rs9299219	1.00[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	nsv831695	chr9:117567626-117726247	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117574600-117586400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:117582400-117587600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:117583200-117587600	Weak transcription	Placenta	Placenta
4	chr9:117583400-117585800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr9:117583400-117585800	Weak transcription	Osteobl	bone
6	chr9:117583400-117586000	Weak transcription	NHLF	lung
7	chr9:117583600-117586400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr9:117584800-117586000	Weak transcription	NHDF-Ad	bronchial
9	chr9:117585200-117585800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr9:117585400-117586000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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