| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2205619-2205950 | Common:5; Rare:152 | ||||
| chr16:2214700-2215120 | Common:3; Rare:153 | ||||
| chr16:2215123-2215162 | Rare:15 | ||||
| chr16:2215196-2215455 | Common:1; Rare:72 | ||||
| chr16:2223146-2223725 | Rare:204 | ||||
| chr16:2223805-2223840 | Rare:16 | ||||
| chr16:2250984-2251237 | Common:1; Rare:63 | ||||
| chr16:2251525-2251827 | Common:1; Rare:107 | ||||
| chr16:2267756-2267916 | Common:3; Rare:54 | ||||
| chr16:2267993-2268247 | Common:1; Rare:119 | ||||
| chr16:2268276-2268467 | Common:3; Rare:59 | ||||
| chr16:2340282-2340334 | Rare:11 | ||||
| chr16:2340636-2340936 | Common:2; Rare:111; Clinvar:3; Clinvar (benign):2 | ||||
| chr16:2428928-2429488 | Common:4; Rare:164 | ||||
| chr16:2459852-2460154 | Common:2; Rare:95 |