Variant report

Variant	rs34947552
Chromosome Location	chr1:220671961-220671962
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220670400-220672200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr1:220670400-220672400	Enhancers	NHEK	skin
3	chr1:220670600-220672200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr1:220670600-220672200	Enhancers	Adipose Nuclei	Adipose
5	chr1:220670600-220672400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:220670600-220672400	Enhancers	HMEC	breast
7	chr1:220670800-220672400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:220671000-220672400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:220671800-220672400	Enhancers	Pancreatic Islets	Pancreatic Islet

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

what's new

Quick links