Variant report

Variant rs10454349
Chromosome Location chr8:91513227-91513228
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:91510000-91516600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr8:91512800-91513600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr8:91512800-91514200 Enhancers Cortex derived primary cultured neurospheres brain
4 chr8:91512800-91514200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
5 chr8:91513000-91513600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr8:91513000-91513600 Enhancers Brain Angular Gyrus brain
7 chr8:91513000-91513800 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr8:91513000-91513800 Enhancers Brain Hippocampus Middle brain
9 chr8:91513000-91514000 Enhancers Brain Substantia Nigra brain
10 chr8:91513000-91514000 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr8:91513200-91513600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr8:91513200-91513600 Enhancers Brain Anterior Caudate brain
13 chr8:91513200-91513800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
14 chr8:91513200-91514000 Active TSS Pancreatic Islets Pancreatic Islet
15 chr8:91513200-91514200 Enhancers Placenta Amnion Placenta Amnion

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