| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:99480769-99481013 | Common:2; Rare:95 | ||||
| chr14:100376273-100376494 | Common:3; Rare:74 | ||||
| chr14:102139684-102139942 | Rare:90 | ||||
| chr14:102362862-102363098 | Rare:104 | ||||
| chr14:103562624-103563048 | Common:8; Rare:166; Clinvar (benign):5 | ||||
| chr14:104970469-104970781 | Common:4; Rare:63 | ||||
| chr14:105021026-105021385 | Common:1; Rare:130 | ||||
| chr15:23565557-23565693 | Rare:42 | ||||
| chr15:30903650-30903936 | Common:2; Rare:76 | ||||
| chr15:32615163-32615660 | Common:6; Rare:121 | ||||
| chr15:34101843-34102083 | Common:1; Rare:48 | ||||
| chr15:34588447-34588588 | Rare:39 | ||||
| chr15:34988236-34988386 | Common:1; Rare:62 | ||||
| chr15:35546128-35546258 | Common:1; Rare:48 | ||||
| chr15:36579323-36579731 | Common:5; Rare:106 |