Variant report
Variant | rs35350728 |
---|---|
Chromosome Location | chr11:16142437-16142438 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:16133800-16146400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr11:16136800-16144000 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
3 | chr11:16137400-16146600 | Weak transcription | Pancreas | Pancrea |
4 | chr11:16138800-16147600 | Weak transcription | Fetal Intestine Small | intestine |
5 | chr11:16140200-16148000 | Weak transcription | Psoas Muscle | Psoas |
6 | chr11:16141200-16147400 | Weak transcription | Brain Germinal Matrix | brain |
7 | chr11:16141200-16147800 | Weak transcription | Fetal Heart | heart |
8 | chr11:16141400-16145800 | Weak transcription | HepG2 | liver |
9 | chr11:16141400-16147600 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
10 | chr11:16141800-16143800 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
11 | chr11:16142000-16143400 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |