Variant report

Variant	rs1928494
Chromosome Location	chr10:93304652-93304653
allele	A/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	chr10:93296200-93312200	Weak transcription	Psoas Muscle	Psoas
2	chr10:93297000-93311400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr10:93297000-93311400	Weak transcription	Left Ventricle	heart
4	chr10:93299400-93311400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr10:93300000-93306600	Enhancers	Fetal Lung	lung
6	chr10:93301000-93314800	Weak transcription	Aorta	Aorta
7	chr10:93302400-93311400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr10:93302600-93308000	Weak transcription	Fetal Brain Male	brain
9	chr10:93302600-93312000	Weak transcription	NHLF	lung
10	chr10:93302800-93305400	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr10:93302800-93307800	Weak transcription	Hela-S3	cervix
12	chr10:93304200-93304800	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr10:93304600-93304800	ZNF genes & repeats	H1 Derived Mesenchymal Stem 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

what's new

Quick links