Variant report

Variant	rs9481715
Chromosome Location	chr6:117761367-117761368
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10081022	0.89[ASN][1000 genomes]
rs72961480	0.89[ASN][1000 genomes]
rs72963407	0.89[ASN][1000 genomes]
rs72967491	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9489143	0.89[ASN][1000 genomes]
rs9489200	0.91[AFR][1000 genomes];1.00[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	nsv532050	chr6:117528154-118203005	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv966655	chr6:117758375-117766294	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:117760000-117762000	Enhancers	Hela-S3	cervix
2	chr6:117760000-117762600	Enhancers	HMEC	breast
3	chr6:117760400-117761400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
4	chr6:117760600-117761400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:117760800-117761400	ZNF genes & repeats	NHEK	skin
6	chr6:117761000-117762000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:117761000-117762600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr6:117761200-117762000	Weak transcription	Osteobl	bone
9	chr6:117761200-117762200	Weak transcription	A549	lung
10	chr6:117761200-117762800	Weak transcription	HSMM	muscle
11	chr6:117761200-117763400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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