| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:102362833-102363103 | Rare:121 | ||||
| chr14:103335493-103335693 | Common:1; Rare:56 | ||||
| chr14:103385197-103385455 | Common:1; Rare:93 | ||||
| chr14:103529070-103529243 | Common:1; Rare:53 | ||||
| chr14:103562618-103563044 | Common:8; Rare:166; Clinvar (benign):5 | ||||
| chr14:103715432-103715823 | Common:1; Rare:125 | ||||
| chr14:105065386-105065614 | Common:1; Rare:43 | ||||
| chr14:105248435-105248602 | Common:4; Rare:78 | ||||
| chr14:105486958-105487205 | Common:3; Rare:58 | ||||
| chr15:22838481-22838750 | Common:2; Rare:108 | ||||
| chr15:25438976-25439167 | Common:3; Rare:72 | ||||
| chr15:34101880-34102150 | Common:1; Rare:47 | ||||
| chr15:34336977-34337332 | Common:2; Rare:90 | ||||
| chr15:34367169-34367352 | Common:2; Rare:81 | ||||
| chr15:34988236-34988450 | Common:1; Rare:87 |