Variant report

Variant rs17072194
Chromosome Location chr13:49346529-49346530
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:49344000-49349000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
2 chr13:49344400-49347400 Weak transcription Hela-S3 cervix
3 chr13:49345800-49348000 Enhancers Dnd41 blood
4 chr13:49346000-49346800 Enhancers Left Ventricle heart
5 chr13:49346000-49346800 Enhancers Right Atrium heart
6 chr13:49346000-49348400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr13:49346200-49346600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr13:49346200-49346800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr13:49346200-49346800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr13:49346200-49346800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr13:49346200-49346800 Enhancers Fetal Heart heart
12 chr13:49346200-49347600 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr13:49346400-49346600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr13:49346400-49346800 Enhancers Fetal Lung lung
15 chr13:49346400-49350600 Weak transcription Breast Myoepithelial Primary Cells Breast

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