Variant report

Variant	rs202162964
Chromosome Location	chr2:115890719-115890720
allele	-/TGTGTATA
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014713	chr2:115858427-116018055	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv3382065	chr2:115889932-115891880	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv1436353	chr2:115890717-115890725	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:115882200-115892400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:115887400-115892600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr2:115887600-115893200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr2:115887600-115893400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr2:115887800-115891200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr2:115889200-115891600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:115889800-115891400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr2:115889800-115891600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr2:115890000-115891000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr2:115890200-115893400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr2:115890400-115893200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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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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