Variant report

Variant rs73006866
Chromosome Location chr1:145551248-145551249
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:145549800-145554200 Weak transcription Placenta Amnion Placenta Amnion
2 chr1:145549800-145558200 Weak transcription Pancreas Pancrea
3 chr1:145549800-145561800 Weak transcription Right Atrium heart
4 chr1:145550000-145554400 Weak transcription Stomach Mucosa stomach
5 chr1:145550200-145551600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr1:145550200-145553200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
7 chr1:145550200-145555000 Weak transcription HMEC breast
8 chr1:145550200-145555200 Weak transcription Esophagus oesophagus
9 chr1:145550200-145556600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr1:145550200-145562200 Weak transcription Right Ventricle heart
11 chr1:145550200-145562400 Weak transcription Brain Angular Gyrus brain
12 chr1:145550400-145551400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr1:145550400-145554400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:145550400-145554600 Weak transcription Breast Myoepithelial Primary Cells Breast
15 chr1:145550400-145556200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
16 chr1:145550400-145562400 Weak transcription Brain Hippocampus Middle brain
17 chr1:145550800-145562000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
18 chr1:145551000-145555800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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