Variant report

Variant rs9808318
Chromosome Location chr2:181890205-181890206
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:181856800-181897200 Weak transcription Primary B cells from cord blood blood
2 chr2:181857800-181901200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr2:181860000-181894800 Weak transcription Primary hematopoietic stem cells blood
4 chr2:181873400-181901000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:181885000-181890600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr2:181886000-181901200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr2:181887800-181890800 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr2:181888200-181891000 Weak transcription HUES64 Cell Line embryonic stem cell
9 chr2:181889800-181891000 Enhancers Fetal Heart heart
10 chr2:181890000-181890400 Enhancers Fetal Lung lung
11 chr2:181890200-181895600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links