Variant report

Variant	rs182946172
Chromosome Location	chr1:215826420-215826421
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	nsv430324	chr1:215649163-216082605	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv873171	chr1:215825167-215925167	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 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	chr1:215823200-215826600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:215824200-215827200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr1:215825200-215827200	Enhancers	Liver	Liver
4	chr1:215825400-215826800	Enhancers	H1 Cell Line	embryonic stem cell
5	chr1:215825800-215827400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr1:215826000-215827000	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr1:215826200-215827200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr1:215826200-215827400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr1:215826400-215827400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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

what's new

Quick links