Variant report

Variant	rs73245952
Chromosome Location	chr8:60540985-60540986
allele	A/T
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:11)

rs_ID	r²[population]
rs10104862	1.00[ASN][1000 genomes]
rs16925082	1.00[ASN][1000 genomes]
rs16925122	1.00[ASN][1000 genomes]
rs16925188	1.00[ASN][1000 genomes]
rs16925218	0.85[ASN][1000 genomes]
rs62504701	1.00[ASN][1000 genomes]
rs62504702	1.00[ASN][1000 genomes]
rs73245958	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73245966	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73245972	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs73680628	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	nsv1030564	chr8:60445016-60752655	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv539630	chr8:60445016-60752655	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60533000-60541200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr8:60537000-60542000	Enhancers	NHDF-Ad	bronchial
3	chr8:60537200-60541600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr8:60538200-60543200	Weak transcription	Fetal Brain Male	brain
5	chr8:60538600-60542000	Weak transcription	Colon Smooth Muscle	Colon
6	chr8:60538800-60541000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr8:60539000-60541000	Weak transcription	HUVEC	blood vessel
8	chr8:60539200-60542000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr8:60539800-60546800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr8:60540000-60542600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:60540000-60542600	Weak transcription	NHLF	lung
12	chr8:60540200-60543200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr8:60540200-60543200	Weak transcription	NH-A	brain
14	chr8:60540400-60542800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr8:60540400-60542800	Weak transcription	Hela-S3	cervix
16	chr8:60540600-60543000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr8:60540800-60541200	Weak transcription	Osteobl	bone

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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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