Variant report

Variant	rs556434835
Chromosome Location	chr2:212159211-212159212
allele	A/C
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	nsv834522	chr2:212066442-212225328	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv433299	chr2:212157104-212161004	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212158800-212159800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr2:212159000-212159600	Enhancers	H1 Cell Line	embryonic stem cell
3	chr2:212159000-212159600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr2:212159000-212159600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:212159000-212160200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr2:212159200-212159600	Enhancers	iPS-15b 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

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