| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2155343-2155634 | Rare:88 | ||||
| chr16:2156047-2156753 | Common:7; Rare:277 | ||||
| chr16:2196450-2197000 | Common:1; Rare:169 | ||||
| chr16:2205287-2205518 | Common:1; Rare:60 | ||||
| chr16:2214770-2215150 | Common:2; Rare:143 | ||||
| chr16:2223284-2223673 | Rare:156 | ||||
| chr16:2251548-2251854 | Common:2; Rare:99 | ||||
| chr16:2268374-2268502 | Common:1; Rare:45 | ||||
| chr16:2340695-2340971 | Common:2; Rare:108; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:2429082-2429458 | Common:2; Rare:118 | ||||
| chr16:2459889-2460153 | Common:1; Rare:89 | ||||
| chr16:2470950-2471350 | Common:2; Rare:115 | ||||
| chr16:2474970-2475165 | Rare:62; Clinvar (benign):2 | ||||
| chr16:2513591-2513999 | Rare:135 | ||||
| chr16:2520198-2520406 | Common:8; Rare:128 |