Variant report

Variant	rs140642017
Chromosome Location	chr8:49725552-49725553
allele	-/AC/ACAC
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	nsv526887	chr8:49724699-49729020	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49723200-49730800	Weak transcription	Spleen	Spleen
2	chr8:49723800-49727000	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr8:49723800-49727200	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr8:49724000-49728600	Weak transcription	Fetal Lung	lung
5	chr8:49724400-49730400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr8:49724600-49727000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:49725400-49726000	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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