| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1971913-1972103 | Common:1; Rare:54 | ||||
| chr16:2047784-2048046 | Rare:123; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2267780-2267881 | Rare:34 | ||||
| chr16:2268072-2268449 | Common:4; Rare:126 | ||||
| chr16:2475015-2475149 | Rare:48 | ||||
| chr16:2519374-2519580 | Common:1; Rare:78 | ||||
| chr16:2682360-2682608 | Rare:111 | ||||
| chr16:2752588-2752711 | Common:1; Rare:51 | ||||
| chr16:2776993-2777397 | Common:3; Rare:148 | ||||
| chr16:2911764-2912024 | Common:3; Rare:89 | ||||
| chr16:3065207-3065424 | Common:3; Rare:59 | ||||
| chr16:3112506-3112642 | Common:2; Rare:34 | ||||
| chr16:3134861-3135162 | Common:3; Rare:86 | ||||
| chr16:3263665-3263851 | Common:1; Rare:49 | ||||
| chr16:3305268-3305545 | Common:3; Rare:92 |