Variant report

Variant	rs185322674
Chromosome Location	chr4:20464390-20464391
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	nsv878741	chr4:20440476-20486230	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3390283	chr4:20464254-20466302	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20449600-20486000	Weak transcription	Fetal Lung	lung
2	chr4:20462800-20464600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:20464000-20464400	Enhancers	NHLF	lung
4	chr4:20464000-20465000	Enhancers	HUVEC	blood vessel
5	chr4:20464000-20465200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:20464000-20465200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr4:20464000-20466000	Enhancers	Osteobl	bone
8	chr4:20464000-20466600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:20464200-20464600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:20464200-20464600	Enhancers	Placenta Amnion	Placenta Amnion
11	chr4:20464200-20464600	Enhancers	NHEK	skin

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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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