Variant report

Variant	rs377065850
Chromosome Location	chr6:139743696-139743697
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	nsv519810	chr6:139742788-139743807	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:139742400-139744000	Enhancers	Left Ventricle	heart
2	chr6:139742400-139745600	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr6:139743000-139744800	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr6:139743200-139745600	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr6:139743400-139743800	Enhancers	Primary B cells from peripheral blood	blood
6	chr6:139743400-139744000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:139743400-139744200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr6:139743400-139744400	Enhancers	Pancreas	Pancrea
9	chr6:139743600-139743800	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr6:139743600-139743800	Enhancers	Primary hematopoietic stem cells	blood
11	chr6:139743600-139743800	Enhancers	Stomach Mucosa	stomach
12	chr6:139743600-139745200	Weak transcription	K562	blood

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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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