Variant report

Variant	rs147062242
Chromosome Location	chr3:109983870-109983871
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877332	chr3:109575764-110186611	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv460816	chr3:109878008-110044601	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv591271	chr3:109878008-110044601	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv829668	chr3:109956403-110095215	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv877334	chr3:109983269-110044601	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	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	chr3:109981800-109985200	Enhancers	Ovary	ovary
2	chr3:109982200-109984000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr3:109982200-109984600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr3:109983200-109984200	Enhancers	H1 Cell Line	embryonic stem cell
5	chr3:109983400-109984800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr3:109983800-109984200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr3:109983800-109984600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr3:109983800-109984600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr3:109983800-109985000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr3:109983800-109985200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr3:109983800-109985600	Enhancers	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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