Variant report

Variant	rs191105943
Chromosome Location	chr3:159428766-159428767
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	esv2560522	chr3:159428123-159429500	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:159426200-159429600	Weak transcription	Right Ventricle	heart
2	chr3:159428400-159430200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr3:159428600-159429000	Enhancers	Left Ventricle	heart
4	chr3:159428600-159429400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr3:159428600-159430200	Enhancers	HMEC	breast
6	chr3:159428600-159430400	Enhancers	HUVEC	blood vessel

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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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