| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100305555-100305728 | Common:3; Rare:45 | ||||
| chr14:100306376-100306781 | Common:3; Rare:140 | ||||
| chr14:100374397-100374457 | Rare:17 | ||||
| chr14:100375296-100375805 | Common:4; Rare:83 | ||||
| chr14:100376121-100376620 | Common:5; Rare:146 | ||||
| chr14:101809677-101809951 | Rare:58 | ||||
| chr14:101809987-101810173 | Rare:39 | ||||
| chr14:101810178-101810471 | Common:2; Rare:54 | ||||
| chr14:101823765-101824025 | Common:1; Rare:47 | ||||
| chr14:101825008-101825184 | Rare:27 | ||||
| chr14:101964365-101964700 | Common:4; Rare:104; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:102086943-102087387 | Common:6; Rare:186 | ||||
| chr14:102139249-102139477 | Rare:92 | ||||
| chr14:102139581-102140017 | Rare:151 | ||||
| chr14:102316898-102317090 | Common:4; Rare:76 |