Variant report

Variant	rs562028928
Chromosome Location	chr11:32634999-32635000
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	esv3424973	chr11:32633425-32664062	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32625400-32637200	Weak transcription	Fetal Heart	heart
2	chr11:32627200-32635000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr11:32628200-32635000	Weak transcription	Liver	Liver
4	chr11:32628200-32635400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr11:32629400-32635200	Weak transcription	Fetal Lung	lung
6	chr11:32633400-32635000	Weak transcription	Fetal Kidney	kidney
7	chr11:32634800-32636000	Enhancers	HepG2	liver

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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

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