| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1964822-1964961 | Common:5; Rare:54 | ||||
| chr16:1971935-1972134 | Common:1; Rare:59 | ||||
| chr16:2009682-2009896 | Common:15; Rare:92 | ||||
| chr16:2047793-2048033 | Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2205678-2205883 | Common:4; Rare:96 | ||||
| chr16:2268072-2268178 | Common:1; Rare:51 | ||||
| chr16:2268353-2268497 | Common:1; Rare:52 | ||||
| chr16:2429129-2429484 | Common:3; Rare:117 | ||||
| chr16:2459963-2460153 | Common:1; Rare:58 | ||||
| chr16:2682350-2682633 | Rare:133 | ||||
| chr16:2777001-2777377 | Common:2; Rare:136 | ||||
| chr16:2980382-2980620 | Common:2; Rare:79 | ||||
| chr16:3020064-3020406 | Rare:104 | ||||
| chr16:3065242-3065493 | Common:5; Rare:69 | ||||
| chr16:3112454-3112595 | Rare:33 |