Variant report

Variant rs170901
Chromosome Location chr19:40532800-40532801
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:40504000-40533800 Weak transcription Placenta Amnion Placenta Amnion
2 chr19:40521200-40540800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr19:40528600-40543800 ZNF genes & repeats Liver Liver
4 chr19:40529000-40543800 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr19:40529200-40543800 ZNF genes & repeats Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr19:40529200-40543800 ZNF genes & repeats Duodenum Smooth Muscle Duodenum
7 chr19:40529400-40533800 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
8 chr19:40529400-40534200 ZNF genes & repeats Adipose Nuclei Adipose
9 chr19:40530600-40543800 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr19:40532400-40534600 ZNF genes & repeats Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr19:40532600-40535000 ZNF genes & repeats Cortex derived primary cultured neurospheres brain
12 chr19:40532800-40533200 ZNF genes & repeats H1 Cell Line embryonic stem cell
13 chr19:40532800-40534000 ZNF genes & repeats Aorta Aorta
14 chr19:40532800-40534200 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived

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