Variant report

Variant rs544779571
Chromosome Location chr2:145439979-145439980
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:145423000-145440600 Weak transcription Primary hematopoietic stem cells blood
2 chr2:145436600-145440800 Weak transcription Fetal Kidney kidney
3 chr2:145438000-145440600 Weak transcription Primary B cells from peripheral blood blood
4 chr2:145438400-145441000 Enhancers NHEK skin
5 chr2:145438600-145440600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr2:145438600-145441000 Enhancers HMEC breast
7 chr2:145438800-145452800 Enhancers Primary monocytes fromperipheralblood blood
8 chr2:145439000-145440200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:145439400-145442000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr2:145439600-145440000 Weak transcription Primary hematopoietic stem cells short term culture blood
11 chr2:145439600-145440400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr2:145439600-145440400 Flanking Active TSS K562 blood
13 chr2:145439600-145440800 Enhancers Primary B cells from cord blood blood
14 chr2:145439800-145440200 Enhancers Duodenum Smooth Muscle Duodenum
15 chr2:145439800-145440200 Enhancers Monocytes-CD14+_RO01746 blood

Quick Search:


  
Input of quick search could be:

what's new

Quick links