Variant report

Variant	rs373487705
Chromosome Location	chr9:84501743-84501744
allele	A/C
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	nsv831639	chr9:84501548-84651151	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:84500200-84501800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:84500400-84501800	Enhancers	Brain Germinal Matrix	brain
3	chr9:84500400-84502600	Enhancers	Fetal Brain Male	brain
4	chr9:84501200-84501800	Enhancers	Fetal Lung	lung
5	chr9:84501400-84501800	Enhancers	Fetal Brain Female	brain

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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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