| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:88467370-88467729 | Common:4; Rare:100 | ||||
| chr15:90233892-90234268 | Common:6; Rare:104 | ||||
| chr15:101277413-101277625 | Common:3; Rare:112 | ||||
| chr16:53606-53897 | Common:7; Rare:90 | ||||
| chr16:1964581-1965059 | Common:16; Rare:219 | ||||
| chr16:2047804-2048018 | Rare:94; Clinvar:2 | ||||
| chr16:2268072-2268171 | Rare:45 | ||||
| chr16:2777240-2777356 | Common:1; Rare:43 | ||||
| chr16:3134839-3135118 | Common:2; Rare:69 | ||||
| chr16:4476273-4476455 | Common:3; Rare:66 | ||||
| chr16:8797631-8797866 | Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:18790276-18790460 | Common:1; Rare:68 | ||||
| chr16:20806440-20806530 | Rare:36 | ||||
| chr16:23641257-23641517 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:25111480-25111762 | Common:2; Rare:66 |