Variant report

Variant rs72856369
Chromosome Location chr2:31359313-31359314
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:31350000-31359600 Weak transcription Pancreas Pancrea
2 chr2:31351600-31359600 Weak transcription Primary hematopoietic stem cells short term culture blood
3 chr2:31353400-31359600 Weak transcription Spleen Spleen
4 chr2:31358600-31359600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr2:31358800-31359400 Enhancers A549 lung
6 chr2:31358800-31359600 Active TSS Breast Myoepithelial Primary Cells Breast
7 chr2:31358800-31359800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr2:31359000-31359400 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
9 chr2:31359000-31359600 Enhancers Brain Germinal Matrix brain
10 chr2:31359200-31359400 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
11 chr2:31359200-31359400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
12 chr2:31359200-31359400 Bivalent/Poised TSS Primary hematopoietic stem cells blood
13 chr2:31359200-31359600 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr2:31359200-31359600 Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr2:31359200-31359800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr2:31359200-31359800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr2:31359200-31359800 Flanking Active TSS HMEC breast
18 chr2:31359200-31360000 Flanking Active TSS NHEK skin
19 chr2:31359200-31360400 Flanking Active TSS Primary neutrophils fromperipheralblood blood

Quick Search:


  
Input of quick search could be:

what's new

Quick links