| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1971888-1972172 | Common:2; Rare:82 | ||||
| chr16:2009757-2009955 | Common:9; Rare:79 | ||||
| chr16:2047717-2048063 | Rare:177; Clinvar:2; Clinvar (benign):7 | ||||
| chr16:2155327-2155496 | Rare:65 | ||||
| chr16:2155664-2155828 | Common:2; Rare:46 | ||||
| chr16:2205683-2205874 | Common:4; Rare:91 | ||||
| chr16:2267660-2268187 | Common:4; Rare:223 | ||||
| chr16:2268372-2268587 | Common:2; Rare:75 | ||||
| chr16:2340695-2341059 | Common:4; Rare:134; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:2429121-2429490 | Common:3; Rare:122 | ||||
| chr16:2459976-2460161 | Common:2; Rare:54 | ||||
| chr16:2475022-2475151 | Rare:46 | ||||
| chr16:2682359-2682622 | Rare:122 | ||||
| chr16:2752052-2752351 | Common:3; Rare:105 | ||||
| chr16:2752490-2752852 | Common:2; Rare:147 |