Variant report

Variant	rs146457154
Chromosome Location	chr3:155828192-155828193
allele	A/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	nsv592084	chr3:155751484-155830578	Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv592085	chr3:155827634-156012679	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155826200-155828200	Enhancers	Fetal Lung	lung
2	chr3:155827400-155828400	Enhancers	Fetal Muscle Leg	muscle
3	chr3:155827600-155828200	Enhancers	Fetal Muscle Trunk	muscle
4	chr3:155827600-155828200	Enhancers	Ovary	ovary
5	chr3:155827600-155828200	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr3:155827800-155828200	Enhancers	Right Atrium	heart
7	chr3:155827800-155828400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr3:155828000-155828200	Enhancers	Adipose Nuclei	Adipose
9	chr3:155828000-155829200	Weak transcription	Pancreas	Pancrea

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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