Variant report

Variant	rs72967827
Chromosome Location	chr11:94449868-94449869
allele	C/T
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	chr11:94447800-94450600	ZNF genes & repeats	NHEK	skin
2	chr11:94448800-94453200	Weak transcription	HMEC	breast
3	chr11:94449400-94450200	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr11:94449600-94450200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:94449600-94450800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
6	chr11:94449600-94451800	Enhancers	HUVEC	blood vessel
7	chr11:94449800-94450000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr11:94449800-94450200	ZNF genes & repeats	Aorta	Aorta
9	chr11:94449800-94450200	Enhancers	Psoas Muscle	Psoas
10	chr11:94449800-94450200	Enhancers	Right Atrium	heart
11	chr11:94449800-94450200	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr11:94449800-94450200	Enhancers	Spleen	Spleen
13	chr11:94449800-94450400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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