| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24213050-24213310 | Rare:77 | ||||
| chr14:24213330-24213622 | Common:3; Rare:165 | ||||
| chr14:24215951-24216093 | Common:1; Rare:50 | ||||
| chr14:24232316-24232690 | Common:16; Rare:173 | ||||
| chr14:24232842-24232978 | Rare:59 | ||||
| chr14:24242269-24242446 | Rare:102; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:24242559-24242787 | Common:2; Rare:111; Clinvar:2; Clinvar (benign):4 | ||||
| chr14:24242990-24243210 | Common:2; Rare:35 | ||||
| chr14:24270940-24271360 | Common:5; Rare:200 | ||||
| chr14:24271415-24271668 | Common:3; Rare:119 | ||||
| chr14:24299672-24299961 | Common:10; Rare:192 | ||||
| chr14:24429850-24430093 | Common:1; Rare:78 | ||||
| chr14:24442659-24443073 | Common:10; Rare:239 | ||||
| chr14:30559044-30559245 | Common:4; Rare:147 | ||||
| chr14:30622190-30622353 | Rare:114 |