Variant report

Variant	rs375570688
Chromosome Location	chr3:143620820-143620821
allele	C/T
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	esv2646891	chr3:143620488-143621943	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143618800-143621400	Enhancers	NHLF	lung
2	chr3:143619200-143621400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr3:143619200-143621400	Enhancers	HMEC	breast
4	chr3:143619400-143621000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:143619400-143621600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:143619600-143621000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr3:143619600-143621400	Enhancers	NHDF-Ad	bronchial

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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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