| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31026177-31026672 | Common:7; Rare:216 | ||||
| chr14:31207403-31208060 | Common:4; Rare:338 | ||||
| chr14:31208053-31208540 | Common:4; Rare:154 | ||||
| chr14:31419770-31420190 | Common:5; Rare:188 | ||||
| chr14:31420283-31420778 | Common:11; Rare:228 | ||||
| chr14:31457385-31457577 | Common:4; Rare:129 | ||||
| chr14:31561089-31561537 | Common:6; Rare:184; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr14:32075883-32077090 | Common:10; Rare:582 | ||||
| chr14:33951054-33951249 | Common:2; Rare:126 | ||||
| chr14:34462193-34462554 | Common:2; Rare:257 | ||||
| chr14:34539619-34539856 | Rare:124 | ||||
| chr14:34630085-34630260 | Common:10; Rare:150 | ||||
| chr14:34713540-34714060 | Common:5; Rare:209; Clinvar:4; Clinvar (benign):2 | ||||
| chr14:34714533-34714781 | Common:3; Rare:91 | ||||
| chr14:34874578-34874753 | Rare:55 |