Variant report

Variant	rs370807351
Chromosome Location	chr10:52653570-52653571
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv971910	chr10:52653523-52661089	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52646800-52654800	Weak transcription	Fetal Intestine Small	intestine
2	chr10:52650200-52654200	Enhancers	Liver	Liver
3	chr10:52653000-52653600	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr10:52653400-52653600	Flanking Bivalent TSS/Enh	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