Variant report

Variant rs767333
Chromosome Location chr14:32186264-32186265
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32162000-32186800 Weak transcription Brain Hippocampus Middle brain
2 chr14:32165600-32188200 Weak transcription Right Ventricle heart
3 chr14:32171000-32186400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
4 chr14:32171000-32200600 Weak transcription Placenta Amnion Placenta Amnion
5 chr14:32172000-32186400 Weak transcription Pancreas Pancrea
6 chr14:32172000-32188200 Weak transcription Duodenum Smooth Muscle Duodenum
7 chr14:32173400-32186400 Weak transcription Esophagus oesophagus
8 chr14:32173400-32189800 Weak transcription Primary B cells from cord blood blood
9 chr14:32173400-32218000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr14:32174600-32200000 Weak transcription Primary T helper naive cells fromperipheralblood blood
11 chr14:32175200-32186600 Weak transcription Primary T cells from cord blood blood
12 chr14:32175200-32186600 Weak transcription Adipose Nuclei Adipose
13 chr14:32175200-32187000 Weak transcription Aorta Aorta
14 chr14:32175400-32187000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr14:32175400-32193400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr14:32175400-32205600 Weak transcription Ovary ovary
17 chr14:32181400-32200600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
18 chr14:32182000-32186600 Weak transcription Breast Myoepithelial Primary Cells Breast
19 chr14:32185600-32187400 Enhancers HepG2 liver
20 chr14:32185800-32187200 Enhancers NHEK skin
21 chr14:32186200-32187200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
22 chr14:32186200-32188200 Enhancers Liver Liver

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