Variant report

Variant	rs200066842
Chromosome Location	chr1:212048361-212048362
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	esv2762218	chr1:212046447-212087682	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212047800-212048400	Enhancers	Fetal Muscle Leg	muscle
2	chr1:212048000-212048600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr1:212048000-212048600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr1:212048000-212048600	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr1:212048200-212048400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:212048200-212048600	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr1:212048200-212048600	Enhancers	Adipose Nuclei	Adipose
8	chr1:212048200-212048600	Enhancers	Liver	Liver

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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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