| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103847525-103847851 | Common:5; Rare:140 | ||||
| chr14:103921469-103921720 | Common:3; Rare:79 | ||||
| chr14:104689479-104689727 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr14:104724100-104724287 | Common:3; Rare:73 | ||||
| chr14:104752524-104752797 | Common:2; Rare:77 | ||||
| chr14:104752973-104753271 | Common:2; Rare:115 | ||||
| chr14:104795641-104795949 | Rare:87 | ||||
| chr14:104800402-104800598 | Rare:55 | ||||
| chr14:104924686-104924922 | Common:1; Rare:48 | ||||
| chr14:104985603-104985844 | Common:4; Rare:98 | ||||
| chr14:105020384-105020567 | Common:6; Rare:49 | ||||
| chr14:105021015-105021762 | Common:4; Rare:243 | ||||
| chr14:105064822-105065011 | Common:1; Rare:45 | ||||
| chr14:105065374-105065569 | Rare:35 | ||||
| chr14:105065581-105065804 | Common:4; Rare:31 |