Variant report

Variant rs4982933
Chromosome Location chr14:24948495-24948496
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:24912800-24950800 Weak transcription Gastric stomach
2 chr14:24922800-24951000 Weak transcription Pancreas Pancrea
3 chr14:24927600-24951000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr14:24928200-24950400 Weak transcription HepG2 liver
5 chr14:24928600-24951000 Weak transcription Placenta Placenta
6 chr14:24928800-24951000 Weak transcription Spleen Spleen
7 chr14:24930800-24951000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr14:24933000-24951400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr14:24941600-24951000 Weak transcription Adipose Nuclei Adipose
10 chr14:24942400-24949800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr14:24942400-24950600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr14:24943000-24951000 Weak transcription Fetal Intestine Large intestine
13 chr14:24945600-24950800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr14:24945600-24951000 Weak transcription Primary hematopoietic stem cells short term culture blood
15 chr14:24945800-24950600 Weak transcription Primary hematopoietic stem cells blood

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