Variant report

Variant rs2340785
Chromosome Location chr1:246690441-246690442
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246690000-246690800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:246690000-246692600 Enhancers Primary Natural Killer cells fromperipheralblood blood
3 chr1:246690400-246690600 Flanking Active TSS Primary hematopoietic stem cells short term culture blood
4 chr1:246690400-246690600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
5 chr1:246690400-246690600 Enhancers Monocytes-CD14+_RO01746 blood
6 chr1:246690400-246690800 Flanking Active TSS HepG2 liver
7 chr1:246690400-246691000 Enhancers Gastric stomach
8 chr1:246690400-246691200 Enhancers Lung lung
9 chr1:246690400-246691400 ZNF genes & repeats GM12878-XiMat blood
10 chr1:246690400-246691600 Enhancers Primary T cells fromperipheralblood blood
11 chr1:246690400-246691600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr1:246690400-246691600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr1:246690400-246691800 ZNF genes & repeats Primary monocytes fromperipheralblood blood
14 chr1:246690400-246693000 Enhancers HMEC breast

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