| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103629682-103629860 | Common:4; Rare:92 | ||||
| chr14:103715252-103715933 | Common:3; Rare:577 | ||||
| chr14:103716273-103716394 | Common:1; Rare:23 | ||||
| chr14:103728828-103729041 | Common:2; Rare:60 | ||||
| chr14:103847452-103847863 | Common:10; Rare:406 | ||||
| chr14:103847880-103848180 | Common:2; Rare:124 | ||||
| chr14:103921402-103921766 | Common:6; Rare:195 | ||||
| chr14:104104754-104105003 | Rare:116 | ||||
| chr14:104138149-104138807 | Common:9; Rare:437 | ||||
| chr14:104689206-104689433 | Rare:54 | ||||
| chr14:104689470-104689708 | Common:3; Rare:159; Clinvar (benign):3 | ||||
| chr14:104689757-104690157 | Common:2; Rare:104 | ||||
| chr14:104724051-104724309 | Common:7; Rare:231; Clinvar:1 | ||||
| chr14:104724540-104724870 | Common:4; Rare:126 | ||||
| chr14:104752530-104752812 | Common:3; Rare:125 |