Variant report
Variant | rs9594191 |
---|---|
Chromosome Location | chr13:37681847-37681848 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:37677800-37682200 | Strong transcription | Primary neutrophils fromperipheralblood | blood |
2 | chr13:37679800-37682800 | Weak transcription | Fetal Stomach | stomach |
3 | chr13:37680200-37682000 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
4 | chr13:37680400-37682000 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
5 | chr13:37680400-37682000 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
6 | chr13:37680400-37682600 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
7 | chr13:37680600-37682000 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
8 | chr13:37681200-37682800 | Weak transcription | Muscle Satellite Cultured Cells | -- |
9 | chr13:37681600-37682000 | Enhancers | H1 Cell Line | embryonic stem cell |
10 | chr13:37681600-37682000 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
11 | chr13:37681600-37682800 | Weak transcription | Colon Smooth Muscle | Colon |
12 | chr13:37681600-37685000 | Enhancers | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |