Variant report

Variant	rs10863558
Chromosome Location	chr1:220690689-220690690
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220687200-220691000	Enhancers	HMEC	breast
2	chr1:220687400-220691000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:220690200-220691600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr1:220690400-220690800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:220690400-220691000	Enhancers	NHEK	skin
6	chr1:220690400-220691200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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