Variant report
Variant | rs1489806 |
---|---|
Chromosome Location | chr1:97445507-97445508 |
allele | A/C/G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:97439800-97451800 | Weak transcription | Fetal Heart | heart |
2 | chr1:97444200-97446000 | Enhancers | Fetal Stomach | stomach |
3 | chr1:97444200-97446600 | Enhancers | Fetal Lung | lung |
4 | chr1:97444400-97447000 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
5 | chr1:97444600-97445600 | Enhancers | Fetal Muscle Leg | muscle |
6 | chr1:97444600-97446600 | Enhancers | Fetal Brain Female | brain |
7 | chr1:97444600-97447000 | Enhancers | Brain Germinal Matrix | brain |
8 | chr1:97444800-97446600 | Enhancers | Cortex derived primary cultured neurospheres | brain |
9 | chr1:97445400-97446000 | Enhancers | Sigmoid Colon | Sigmoid Colon |
10 | chr1:97445400-97446400 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
11 | chr1:97445400-97450600 | Weak transcription | Pancreatic Islets | Pancreatic Islet |