| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1971932-1972081 | Common:1; Rare:42 | ||||
| chr16:2047790-2048038 | Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155338-2155503 | Rare:54 | ||||
| chr16:2268069-2268186 | Common:1; Rare:56 | ||||
| chr16:2459976-2460146 | Common:1; Rare:49 | ||||
| chr16:2682350-2682631 | Rare:133 | ||||
| chr16:2777235-2777377 | Common:1; Rare:57 | ||||
| chr16:3020249-3020377 | Rare:49 | ||||
| chr16:3024284-3024484 | Common:2; Rare:77 | ||||
| chr16:3065190-3065467 | Common:4; Rare:75 | ||||
| chr16:3134861-3135121 | Common:2; Rare:65 | ||||
| chr16:3305400-3305518 | Common:1; Rare:40 | ||||
| chr16:3305725-3305944 | Common:3; Rare:60 | ||||
| chr16:3400967-3401226 | Common:6; Rare:95 | ||||
| chr16:3443450-3443745 | Common:3; Rare:101 |