Variant report

Variant rs1439608
Chromosome Location chr5:124569398-124569399
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:124546600-124585200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr5:124561400-124572600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr5:124567400-124569600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr5:124567800-124570000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr5:124568000-124569800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr5:124568000-124570000 Enhancers Fetal Adrenal Gland Adrenal Gland
7 chr5:124568200-124569800 Enhancers Pancreatic Islets Pancreatic Islet
8 chr5:124568200-124570200 Enhancers Stomach Mucosa stomach
9 chr5:124568600-124569600 Enhancers Brain Substantia Nigra brain
10 chr5:124568600-124573400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr5:124568800-124571000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr5:124568800-124571600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
13 chr5:124568800-124571600 Weak transcription Brain Anterior Caudate brain
14 chr5:124569200-124569800 Enhancers Brain Angular Gyrus brain
15 chr5:124569200-124570200 Enhancers Fetal Heart heart

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