Variant report
Variant | rs71482998 |
---|---|
Chromosome Location | chr11:16127188-16127189 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:16098600-16137000 | Weak transcription | Pancreas | Pancrea |
2 | chr11:16119600-16130200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
3 | chr11:16120800-16130800 | Weak transcription | Esophagus | oesophagus |
4 | chr11:16121600-16135400 | Weak transcription | Fetal Intestine Large | intestine |
5 | chr11:16121800-16136800 | Weak transcription | Small Intestine | intestine |
6 | chr11:16122400-16132400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
7 | chr11:16126800-16128000 | ZNF genes & repeats | Cortex derived primary cultured neurospheres | brain |
8 | chr11:16126800-16128600 | ZNF genes & repeats | Ganglion Eminence derived primary cultured neurospheres | brain |
9 | chr11:16127000-16127400 | ZNF genes & repeats | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
10 | chr11:16127000-16127400 | ZNF genes & repeats | Liver | Liver |