Variant report

Variant rs12064317
Chromosome Location chr1:215227041-215227042
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:215221200-215227600 Weak transcription HUES48 Cell Line embryonic stem cell
2 chr1:215222800-215242200 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr1:215225600-215227200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr1:215225600-215229000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr1:215226400-215227800 Weak transcription HUES64 Cell Line embryonic stem cell
6 chr1:215226600-215227600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
7 chr1:215226800-215228600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr1:215226800-215228600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr1:215226800-215228600 Weak transcription NHLF lung
10 chr1:215226800-215230000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr1:215226800-215230400 Weak transcription Osteobl bone
12 chr1:215227000-215227400 Weak transcription NHDF-Ad bronchial

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