Variant report

Variant	rs16893808
Chromosome Location	chr8:96307937-96307938
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96307000-96309200	Enhancers	Placenta	Placenta
2	chr8:96307400-96308000	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr8:96307600-96308000	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr8:96307600-96308000	Enhancers	Liver	Liver
5	chr8:96307600-96308000	Active TSS	Duodenum Mucosa	Duodenum
6	chr8:96307600-96308000	Active TSS	Duodenum Smooth Muscle	Duodenum
7	chr8:96307600-96308000	Active TSS	Rectal Mucosa Donor 29	rectum
8	chr8:96307600-96308000	Enhancers	NH-A	brain
9	chr8:96307600-96308200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr8:96307600-96308200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr8:96307600-96308200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr8:96307600-96308200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr8:96307600-96308200	Active TSS	Ovary	ovary
14	chr8:96307800-96308000	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr8:96307800-96308000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:96307800-96308200	Active TSS	Fetal Lung	lung

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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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