| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87949476-87949499 | Rare:5 | ||||
| chr16:87949667-87949702 | Rare:7 | ||||
| chr16:87949923-87950311 | Common:5; Rare:124 | ||||
| chr16:87950324-87950542 | Common:1; Rare:48 | ||||
| chr16:87950734-87951163 | Common:4; Rare:98 | ||||
| chr16:87951225-87951699 | Common:3; Rare:190 | ||||
| chr16:88452622-88452850 | Common:4; Rare:55 | ||||
| chr16:88453063-88453402 | Common:3; Rare:132 | ||||
| chr16:88570103-88570510 | Common:2; Rare:154 | ||||
| chr16:88570811-88571119 | Common:1; Rare:97 | ||||
| chr16:88650418-88650539 | Common:1; Rare:53 | ||||
| chr16:88650927-88651242 | Common:1; Rare:110; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:88662982-88663436 | Common:11; Rare:210 | ||||
| chr16:88686412-88686807 | Common:4; Rare:147 | ||||
| chr16:88686835-88686930 | Rare:31 |