Variant report

Variant	rs567271671
Chromosome Location	chr14:84294489-84294490
allele	G/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	esv2751287	chr14:84294487-84338247	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84292800-84294600	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr14:84293200-84295000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr14:84293400-84295400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr14:84293800-84294800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr14:84294200-84295000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr14:84294400-84295200	Weak transcription	iPS-20b 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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