Variant report
Variant | rs10020568 |
---|---|
Chromosome Location | chr4:53426734-53426735 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:53417800-53427000 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr4:53419400-53426800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
3 | chr4:53421400-53426800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
4 | chr4:53421600-53434000 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
5 | chr4:53421800-53426800 | Weak transcription | Fetal Heart | heart |
6 | chr4:53422000-53426800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
7 | chr4:53422000-53426800 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
8 | chr4:53422000-53427000 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
9 | chr4:53423400-53429800 | Weak transcription | Gastric | stomach |
10 | chr4:53426400-53427800 | Enhancers | HMEC | breast |
11 | chr4:53426600-53427600 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
12 | chr4:53426600-53427800 | Enhancers | Osteobl | bone |
13 | chr4:53426600-53428000 | Enhancers | NHEK | skin |