Variant report

Variant	rs139751642
Chromosome Location	chr2:181736600-181736601
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	nsv963752	chr2:181734234-181756646	Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 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	chr2:181736400-181736600	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr2:181736400-181737000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:181736400-181737200	Enhancers	NHDF-Ad	bronchial
4	chr2:181736400-181738200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr2:181736600-181737000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:181736600-181737000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
7	chr2:181736600-181737200	Enhancers	HSMMtube	muscle
8	chr2:181736600-181737200	Enhancers	NHLF	lung

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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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