| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:92121658-92121990 | Common:4; Rare:109 | ||||
| chr14:93184851-93185001 | Rare:48 | ||||
| chr14:93207038-93207288 | Common:2; Rare:123 | ||||
| chr14:94081141-94081328 | Common:4; Rare:62 | ||||
| chr14:96363333-96363554 | Common:1; Rare:73 | ||||
| chr14:96502301-96502446 | Rare:56 | ||||
| chr14:99480788-99480986 | Common:2; Rare:79 | ||||
| chr14:100376264-100376502 | Common:3; Rare:79 | ||||
| chr14:102139647-102139914 | Rare:91 | ||||
| chr14:102362862-102363092 | Rare:103 | ||||
| chr14:103333924-103334253 | Common:3; Rare:140 | ||||
| chr14:103562624-103563266 | Common:11; Rare:264; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103715442-103715858 | Common:1; Rare:140 | ||||
| chr14:105021031-105021386 | Common:1; Rare:127 | ||||
| chr15:22838356-22838737 | Common:3; Rare:135 |