Variant report

Variant	rs73861314
Chromosome Location	chr3:133796991-133796992
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133792200-133802600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:133794600-133797600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr3:133795200-133798000	Enhancers	Hela-S3	cervix
4	chr3:133795800-133797000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr3:133796200-133797600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr3:133796200-133798800	Enhancers	NHDF-Ad	bronchial
7	chr3:133796400-133797200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr3:133796400-133798200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr3:133796600-133798200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr3:133796600-133798200	Enhancers	Placenta	Placenta
11	chr3:133796600-133798200	Enhancers	NHLF	lung
12	chr3:133796600-133798400	Enhancers	Adipose Nuclei	Adipose
13	chr3:133796600-133798600	Enhancers	Osteobl	bone

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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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