Variant report
Variant | rs10766299 |
---|---|
Chromosome Location | chr11:16174802-16174803 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:16170800-16175800 | Weak transcription | Muscle Satellite Cultured Cells | -- |
2 | chr11:16171000-16175200 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
3 | chr11:16171600-16175600 | Weak transcription | Fetal Intestine Large | intestine |
4 | chr11:16172400-16176000 | Weak transcription | Fetal Intestine Small | intestine |
5 | chr11:16172400-16191400 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
6 | chr11:16172600-16191400 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
7 | chr11:16173400-16175600 | Enhancers | HepG2 | liver |
8 | chr11:16173800-16175400 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
9 | chr11:16174200-16175200 | Weak transcription | HMEC | breast |
10 | chr11:16174200-16191200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
11 | chr11:16174600-16176800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
12 | chr11:16174800-16175600 | Enhancers | A549 | lung |
13 | chr11:16174800-16178400 | Enhancers | Stomach Mucosa | stomach |
14 | chr11:16174800-16180000 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |