| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2340715-2341034 | Common:1; Rare:122; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:2428934-2428995 | Rare:14 | ||||
| chr16:2429018-2429497 | Common:4; Rare:149 | ||||
| chr16:2459633-2459770 | Rare:30 | ||||
| chr16:2459855-2460195 | Common:2; Rare:107 | ||||
| chr16:2471155-2471312 | Rare:35 | ||||
| chr16:2474925-2475193 | Rare:87; Clinvar (benign):5 | ||||
| chr16:2513546-2514081 | Rare:210 | ||||
| chr16:2514160-2514217 | Rare:20 | ||||
| chr16:2520095-2520477 | Common:9; Rare:197 | ||||
| chr16:2520891-2520998 | Rare:50 | ||||
| chr16:2531851-2532212 | Common:2; Rare:144 | ||||
| chr16:2537456-2537612 | Rare:34 | ||||
| chr16:2537824-2538144 | Common:3; Rare:117 | ||||
| chr16:2681998-2682141 | Common:1; Rare:37 |