Variant report

Variant rs12105820
Chromosome Location chr2:31125055-31125056
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:31120000-31133600 Weak transcription Primary B cells from cord blood blood
2 chr2:31120400-31126000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr2:31121600-31126200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr2:31121600-31133200 Weak transcription Primary hematopoietic stem cells blood
5 chr2:31121800-31127400 Strong transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr2:31122200-31143800 Weak transcription Esophagus oesophagus
7 chr2:31122800-31125800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr2:31122800-31191400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:31124400-31133600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr2:31124600-31125400 Strong transcription Breast Myoepithelial Primary Cells Breast
11 chr2:31124600-31146800 Weak transcription NHEK skin
12 chr2:31125000-31126200 Strong transcription Primary hematopoietic stem cells short term culture blood
13 chr2:31125000-31127200 Strong transcription Primary neutrophils fromperipheralblood blood
14 chr2:31125000-31133200 Weak transcription A549 lung

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