Variant report

Variant	rs550719488
Chromosome Location	chr4:147878026-147878027
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	esv1826357	chr4:147876484-147900981	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147867600-147880600	Weak transcription	Pancreas	Pancrea
2	chr4:147876400-147880000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:147877400-147879000	Enhancers	NHDF-Ad	bronchial
4	chr4:147877600-147878800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:147877600-147879000	Enhancers	Muscle Satellite Cultured Cells	--
6	chr4:147877600-147882600	Enhancers	Hela-S3	cervix
7	chr4:147877800-147879000	Enhancers	HUVEC	blood vessel
8	chr4:147878000-147878600	Enhancers	HMEC	breast
9	chr4:147878000-147879200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:147878000-147879200	Enhancers	NH-A	brain
11	chr4:147878000-147879200	Enhancers	NHEK	skin
12	chr4:147878000-147879200	Enhancers	Osteobl	bone

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

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