Variant report

Variant rs12408537
Chromosome Location chr1:94227085-94227086
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94219800-94231600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr1:94220000-94254200 Weak transcription Aorta Aorta
3 chr1:94222400-94228200 Enhancers Primary Natural Killer cells fromperipheralblood blood
4 chr1:94223000-94237000 Weak transcription NHEK skin
5 chr1:94223600-94229200 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:94224800-94228000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr1:94225000-94231800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
8 chr1:94225000-94233600 Weak transcription Right Atrium heart
9 chr1:94225400-94231600 Weak transcription Thymus Thymus
10 chr1:94225600-94227600 Weak transcription HMEC breast
11 chr1:94225600-94230400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:94225600-94233600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr1:94225600-94233800 Weak transcription Fetal Lung lung
14 chr1:94226400-94230200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr1:94226600-94228800 Weak transcription Placenta Placenta
16 chr1:94226800-94227200 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
17 chr1:94227000-94227200 Weak transcription Lung lung
18 chr1:94227000-94228400 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
19 chr1:94227000-94231800 Weak transcription HepG2 liver

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