| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:39432760-39433040 | Rare:134 | ||||
| chr14:44897003-44897346 | Common:2; Rare:207 | ||||
| chr14:44961886-44962268 | Common:6; Rare:222 | ||||
| chr14:45083924-45084191 | Common:2; Rare:192 | ||||
| chr14:45135520-45136042 | Common:2; Rare:160 | ||||
| chr14:45253039-45253398 | Common:1; Rare:177 | ||||
| chr14:45253348-45253748 | Common:3; Rare:174 | ||||
| chr14:49586320-49586790 | Common:2; Rare:435; Clinvar (benign):1 | ||||
| chr14:49598603-49599066 | Common:8; Rare:331 | ||||
| chr14:49599100-49599340 | Rare:111 | ||||
| chr14:49620160-49620490 | Rare:91 | ||||
| chr14:49620570-49620856 | Common:4; Rare:222; Clinvar:7 | ||||
| chr14:49634275-49634918 | Common:2; Rare:291; Clinvar:26; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr14:49688150-49688312 | Rare:89 | ||||
| chr14:49693022-49693170 | Common:1; Rare:49 |