| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3443461-3443757 | Common:3; Rare:108 | ||||
| chr16:3457914-3458114 | Common:2; Rare:98 | ||||
| chr16:3577354-3577486 | Common:3; Rare:32 | ||||
| chr16:3611554-3611788 | Rare:102; Clinvar:1 | ||||
| chr16:3717517-3717630 | Rare:57 | ||||
| chr16:4351250-4351513 | Common:2; Rare:116 | ||||
| chr16:4425494-4425884 | Common:3; Rare:145 | ||||
| chr16:4476227-4476448 | Common:3; Rare:82 | ||||
| chr16:4538765-4538992 | Rare:84 | ||||
| chr16:4624639-4624869 | Common:1; Rare:91 | ||||
| chr16:4734199-4734298 | Common:1; Rare:33 | ||||
| chr16:4767122-4767330 | Common:1; Rare:69 | ||||
| chr16:5071758-5071849 | Rare:40; Clinvar (benign):1 | ||||
| chr16:8797621-8797866 | Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:8868983-8869261 | Common:4; Rare:123 |