Variant report

Variant	rs372765749
Chromosome Location	chr10:52653566-52653567
allele	A/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

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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