| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:25257399-25257724 | Common:4; Rare:116 | ||||
| chr16:25257785-25258395 | Common:14; Rare:285 | ||||
| chr16:25691544-25691736 | Common:2; Rare:42 | ||||
| chr16:25691872-25692091 | Common:1; Rare:61 | ||||
| chr16:27203373-27203585 | Rare:73 | ||||
| chr16:27203606-27204111 | Common:5; Rare:162 | ||||
| chr16:27268219-27268263 | Rare:9 | ||||
| chr16:27268631-27268929 | Common:1; Rare:102 | ||||
| chr16:27313815-27313943 | Rare:34 | ||||
| chr16:27427141-27427298 | Rare:24 | ||||
| chr16:27549854-27550230 | Common:2; Rare:151 | ||||
| chr16:28211840-28212372 | Common:5; Rare:171 | ||||
| chr16:28292016-28292146 | Rare:27 | ||||
| chr16:28292188-28292630 | Common:2; Rare:109 | ||||
| chr16:28491940-28492246 | Common:1; Rare:70; Clinvar:4; Clinvar (benign):2 |