Variant report

Variant	rs566399648
Chromosome Location	chr21:16537747-16537748
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063385	chr21:16521617-16926212	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv913413	chr21:16537728-16621859	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16536600-16537800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr21:16536600-16538000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr21:16536600-16538400	Enhancers	HepG2	liver
4	chr21:16536800-16537800	Enhancers	Fetal Heart	heart
5	chr21:16536800-16537800	Enhancers	Hela-S3	cervix
6	chr21:16536800-16538000	Enhancers	HMEC	breast
7	chr21:16537200-16537800	Enhancers	Fetal Intestine Large	intestine
8	chr21:16537400-16538000	Enhancers	Fetal Intestine Small	intestine
9	chr21:16537400-16546000	Weak transcription	Pancreas	Pancrea

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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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