| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:104579718-104579784 | Rare:12 | ||||
| chr14:104772375-104772694 | Common:5; Rare:83; Clinvar:2; Clinvar (benign):4 | ||||
| chr14:104970469-104970567 | Common:2; Rare:20 | ||||
| chr14:105300996-105301117 | Rare:26 | ||||
| chr14:105315509-105315627 | Rare:22 | ||||
| chr14:105419362-105419442 | Rare:13 | ||||
| chr14:105419728-105420027 | Rare:91 | ||||
| chr14:105486972-105487251 | Common:3; Rare:78 | ||||
| chr15:22838356-22838823 | Common:3; Rare:158 | ||||
| chr15:25438984-25439209 | Common:2; Rare:84 | ||||
| chr15:29269776-29269874 | Rare:39 | ||||
| chr15:29822024-29822248 | Rare:80 | ||||
| chr15:30624094-30624374 | Common:2; Rare:40 | ||||
| chr15:30903748-30903954 | Common:1; Rare:55 | ||||
| chr15:31327844-31328160 | Common:1; Rare:121 |