Variant report

Variant	rs567446567
Chromosome Location	chr5:114641642-114641643
allele	G/T
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	nsv980960	chr5:114640484-114645980	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114632200-114641800	Weak transcription	Stomach Mucosa	stomach
2	chr5:114641600-114642000	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr5:114641600-114642200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr5:114641600-114642200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:114641600-114642200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr5:114641600-114642400	Enhancers	Rectal Mucosa Donor 31	rectum

Quick Search:

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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