| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:70809480-70810016 | Common:18; Rare:620 | ||||
| chr14:70907120-70907834 | Common:11; Rare:630 | ||||
| chr14:71320159-71320559 | Rare:490 | ||||
| chr14:71320561-71321263 | Common:15; Rare:621 | ||||
| chr14:72742040-72742550 | Common:9; Rare:203 | ||||
| chr14:72892802-72893730 | Common:25; Rare:436 | ||||
| chr14:72893975-72894375 | Common:23; Rare:396 | ||||
| chr14:72894492-72894936 | Common:8; Rare:113 | ||||
| chr14:72925789-72926548 | Common:42; Rare:669 | ||||
| chr14:72926581-72926807 | Common:2; Rare:71 | ||||
| chr14:72927065-72927465 | Common:8; Rare:129 | ||||
| chr14:73026598-73026998 | Common:4; Rare:77 | ||||
| chr14:73027019-73027427 | Common:10; Rare:505 | ||||
| chr14:73058192-73059002 | Common:22; Rare:877 | ||||
| chr14:73136161-73137075 | Common:18; Rare:535; Clinvar:12; Clinvar (benign):4 |