Variant report
Variant | rs913277 |
---|---|
Chromosome Location | chr9:96910136-96910137 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:96903000-96912000 | Weak transcription | HepG2 | liver |
2 | chr9:96903800-96910800 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
3 | chr9:96904000-96912800 | Weak transcription | NH-A | brain |
4 | chr9:96904000-96927200 | Weak transcription | Thymus | Thymus |
5 | chr9:96904400-96912600 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
6 | chr9:96904600-96913200 | Weak transcription | Adipose Nuclei | Adipose |
7 | chr9:96904800-96910200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
8 | chr9:96904800-96912000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
9 | chr9:96904800-96912000 | Weak transcription | Spleen | Spleen |
10 | chr9:96906800-96911000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
11 | chr9:96907200-96912200 | Weak transcription | Fetal Muscle Leg | muscle |
12 | chr9:96907400-96913200 | Weak transcription | Lung | lung |
13 | chr9:96909000-96910600 | Enhancers | NHEK | skin |
14 | chr9:96909400-96913000 | Weak transcription | Placenta Amnion | Placenta Amnion |
15 | chr9:96910000-96910400 | Flanking Active TSS | Foreskin Keratinocyte Primary Cells skin02 | Skin |
16 | chr9:96910000-96911000 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
17 | chr9:96910000-96911000 | Enhancers | Esophagus | oesophagus |