Variant report

Variant	rs538561713
Chromosome Location	chr5:114641824-114641825
allele	C/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:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114641600-114642000	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr5:114641600-114642200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr5:114641600-114642200	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr5:114641600-114642200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr5:114641600-114642400	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr5:114641800-114642000	Flanking Bivalent TSS/Enh	Pancreas	Pancrea
7	chr5:114641800-114642200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr5:114641800-114642200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr5:114641800-114642200	Enhancers	Fetal Intestine Small	intestine
10	chr5:114641800-114642200	Enhancers	Stomach Mucosa	stomach
11	chr5:114641800-114642400	Enhancers	Brain Germinal Matrix	brain
12	chr5:114641800-114642600	Enhancers	Duodenum Mucosa	Duodenum

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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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