| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:23183150-23183209 | Rare:5 | ||||
| chr16:23302673-23302775 | Common:2; Rare:23 | ||||
| chr16:23453099-23453262 | Rare:48 | ||||
| chr16:23509875-23510012 | Common:1; Rare:27 | ||||
| chr16:23510299-23510750 | Common:6; Rare:178 | ||||
| chr16:23510762-23510846 | Rare:19 | ||||
| chr16:23557101-23557182 | Common:1; Rare:32 | ||||
| chr16:23557238-23557405 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:23557598-23557839 | Common:1; Rare:98 | ||||
| chr16:23557985-23558055 | Rare:26 | ||||
| chr16:23558078-23558166 | Rare:40 | ||||
| chr16:23596226-23596513 | Common:1; Rare:80 | ||||
| chr16:23640153-23640422 | Common:1; Rare:54 | ||||
| chr16:23641097-23641548 | Common:3; Rare:147; Clinvar:13; Clinvar (benign):19; Clinvar (pathogenic):4 | ||||
| chr16:23678608-23678979 | Common:5; Rare:108 |