Variant report

Variant rs35396435
Chromosome Location chr14:24942735-24942736
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:24912800-24950800 Weak transcription Gastric stomach
2 chr14:24922200-24946000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr14:24922800-24951000 Weak transcription Pancreas Pancrea
4 chr14:24927600-24951000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr14:24928200-24950400 Weak transcription HepG2 liver
6 chr14:24928600-24951000 Weak transcription Placenta Placenta
7 chr14:24928800-24951000 Weak transcription Spleen Spleen
8 chr14:24930800-24951000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr14:24933000-24951400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr14:24935400-24948400 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr14:24941600-24951000 Weak transcription Adipose Nuclei Adipose
12 chr14:24942400-24949800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr14:24942400-24950600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --

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