Variant report

Variant	rs72926298
Chromosome Location	chr4:103309209-103309210
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103308000-103312800	Weak transcription	Placenta	Placenta
2	chr4:103308600-103309800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:103308800-103309400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:103308800-103310200	Enhancers	Hela-S3	cervix
5	chr4:103308800-103312400	Enhancers	HMEC	breast
6	chr4:103309000-103310200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:103309000-103310200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:103309000-103312200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:103309000-103312400	Enhancers	NHEK	skin
10	chr4:103309200-103311800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

Quick Search:

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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