Variant report

Variant	rs567541135
Chromosome Location	chr13:30194745-30194746
allele	G/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	nsv528336	chr13:30194288-30226498	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30193400-30196400	Enhancers	NHDF-Ad	bronchial
2	chr13:30193800-30196400	Enhancers	Muscle Satellite Cultured Cells	--
3	chr13:30193800-30197000	Enhancers	Osteobl	bone
4	chr13:30194000-30195600	Enhancers	HSMM	muscle
5	chr13:30194200-30195600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr13:30194200-30195600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr13:30194200-30196400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr13:30194400-30194800	Flanking Active TSS	NH-A	brain
9	chr13:30194400-30196600	Enhancers	NHEK	skin
10	chr13:30194600-30194800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr13:30194600-30195000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr13:30194600-30195000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr13:30194600-30196400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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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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