| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:38256056-38256185 | Common:1; Rare:37 | ||||
| chr14:39266819-39267418 | Common:3; Rare:204 | ||||
| chr14:39432418-39432650 | Common:6; Rare:79 | ||||
| chr14:44961892-44962259 | Common:3; Rare:106 | ||||
| chr14:45135723-45135979 | Common:1; Rare:48 | ||||
| chr14:45253134-45253291 | Rare:38 | ||||
| chr14:49586292-49586766 | Common:1; Rare:241; Clinvar (benign):1 | ||||
| chr14:49598731-49599023 | Common:1; Rare:107 | ||||
| chr14:49620570-49620812 | Common:2; Rare:97 | ||||
| chr14:49892898-49893128 | Rare:97 | ||||
| chr14:50312146-50312374 | Rare:99 | ||||
| chr14:50668277-50668556 | Common:3; Rare:102 | ||||
| chr14:50944405-50944538 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51651627-51651973 | Common:4; Rare:97 | ||||
| chr14:52069000-52069224 | Common:2; Rare:50 |