Variant report

Variant	rs7920599
Chromosome Location	chr10:4824425-4824426
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs7068449	1.00[AMR][1000 genomes]
rs7903328	1.00[AMR][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	nsv894787	chr10:4385379-4857717	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4823000-4829800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:4823200-4824600	Enhancers	HUVEC	blood vessel
3	chr10:4824000-4824600	Enhancers	Pancreas	Pancrea
4	chr10:4824000-4824600	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr10:4824000-4824600	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr10:4824000-4824800	Enhancers	Psoas Muscle	Psoas
7	chr10:4824000-4827200	Weak transcription	NHDF-Ad	bronchial
8	chr10:4824400-4829000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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