| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100375287-100375755 | Common:4; Rare:79 | ||||
| chr14:100376259-100376489 | Common:3; Rare:76 | ||||
| chr14:102086987-102087452 | Common:5; Rare:199 | ||||
| chr14:102139658-102139923 | Rare:93 | ||||
| chr14:102362847-102363092 | Rare:112 | ||||
| chr14:103333931-103334252 | Common:3; Rare:133 | ||||
| chr14:103529072-103529205 | Common:1; Rare:36 | ||||
| chr14:103562624-103563066 | Common:8; Rare:177; Clinvar (benign):5 | ||||
| chr14:103715482-103715869 | Common:1; Rare:125 | ||||
| chr14:105021003-105021396 | Common:1; Rare:143 | ||||
| chr14:105419765-105420008 | Rare:72 | ||||
| chr15:30903718-30903952 | Common:1; Rare:60 | ||||
| chr15:32615163-32615611 | Common:6; Rare:107 | ||||
| chr15:34101821-34102113 | Common:1; Rare:64 | ||||
| chr15:34582857-34582902 | Rare:17 |