Variant report

Variant rs149458713
Chromosome Location chr12:47030604-47030605
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:47022000-47030800 Weak transcription Placenta Amnion Placenta Amnion
2 chr12:47023200-47032400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr12:47024000-47030800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr12:47025000-47030800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr12:47025400-47034000 Weak transcription Skeletal Muscle Female skeletal muscle
6 chr12:47025800-47032200 Weak transcription NHEK skin
7 chr12:47026000-47030800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr12:47026000-47035200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr12:47027400-47032400 Weak transcription Gastric stomach
10 chr12:47030200-47030800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr12:47030200-47034000 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr12:47030600-47031400 ZNF genes & repeats Primary Natural Killer cells fromperipheralblood blood
13 chr12:47030600-47031800 ZNF genes & repeats Primary hematopoietic stem cells blood
14 chr12:47030600-47032400 ZNF genes & repeats Dnd41 blood

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