Variant report

Variant	rs374491007
Chromosome Location	chr6:139743378-139743379
allele	C/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:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:139741000-139743400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr6:139741000-139743400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:139741200-139743400	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr6:139741800-139743600	Enhancers	Ovary	ovary
5	chr6:139742400-139743400	Weak transcription	Pancreas	Pancrea
6	chr6:139742400-139744000	Enhancers	Left Ventricle	heart
7	chr6:139742400-139745600	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr6:139743000-139743400	Weak transcription	K562	blood
9	chr6:139743000-139744800	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr6:139743200-139745600	Enhancers	Primary monocytes fromperipheralblood	blood

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

what's new

Quick links