Variant report

Variant rs61609009
Chromosome Location chr14:78721856-78721857
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:78710200-78729800 Weak transcription Brain Inferior Temporal Lobe brain
2 chr14:78719600-78722200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr14:78719800-78722200 Enhancers NH-A brain
4 chr14:78720200-78722200 Enhancers NHEK skin
5 chr14:78720600-78722200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr14:78721000-78722000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr14:78721000-78722000 Enhancers Brain Germinal Matrix brain
8 chr14:78721000-78722400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr14:78721200-78722000 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr14:78721200-78722000 Enhancers NHLF lung
11 chr14:78721600-78722200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr14:78721600-78722400 Enhancers Fetal Brain Male brain
13 chr14:78721800-78725800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr14:78721800-78730400 Weak transcription Brain Angular Gyrus brain

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