| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31561291-31561667 | Common:2; Rare:119; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:32076245-32076316 | Rare:21 | ||||
| chr14:32076814-32077093 | Common:3; Rare:93 | ||||
| chr14:32077094-32077358 | Common:1; Rare:55 | ||||
| chr14:33950938-33951366 | Common:2; Rare:123 | ||||
| chr14:34018280-34018351 | Common:2; Rare:12 | ||||
| chr14:34018592-34018887 | Common:1; Rare:47 | ||||
| chr14:34462124-34462609 | Common:1; Rare:177 | ||||
| chr14:34539569-34539875 | Common:1; Rare:94 | ||||
| chr14:34630085-34630365 | Common:6; Rare:108 | ||||
| chr14:34714396-34714810 | Common:5; Rare:149 | ||||
| chr14:34714870-34715006 | Common:1; Rare:28 | ||||
| chr14:34874391-34874494 | Common:1; Rare:32 | ||||
| chr14:34874824-34875014 | Common:2; Rare:58 | ||||
| chr14:34875307-34875579 | Common:1; Rare:95 |