| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1971800-1972110 | Common:3; Rare:91 | ||||
| chr16:2047795-2048038 | Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155482-2155815 | Common:1; Rare:98 | ||||
| chr16:2268069-2268178 | Common:1; Rare:54 | ||||
| chr16:2429156-2429478 | Common:2; Rare:102 | ||||
| chr16:2459974-2460133 | Rare:41 | ||||
| chr16:2474983-2475151 | Rare:53 | ||||
| chr16:2777125-2777380 | Common:2; Rare:105 | ||||
| chr16:2911739-2912018 | Common:3; Rare:97 | ||||
| chr16:2980394-2980584 | Common:1; Rare:61 | ||||
| chr16:3020064-3020442 | Rare:118 | ||||
| chr16:3112492-3112617 | Common:2; Rare:29 | ||||
| chr16:3134841-3135153 | Common:3; Rare:86 | ||||
| chr16:3263660-3263768 | Common:1; Rare:30 | ||||
| chr16:3305392-3305524 | Common:1; Rare:46 |