| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35291646-35291909 | Common:7; Rare:48 | ||||
| chr14:35291992-35292484 | Common:7; Rare:143; Clinvar:1 | ||||
| chr14:35403921-35404270 | Common:2; Rare:117 | ||||
| chr14:35404406-35404457 | Rare:15 | ||||
| chr14:35404594-35404928 | Common:2; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:35405054-35405274 | Common:1; Rare:44 | ||||
| chr14:35533869-35534183 | Common:3; Rare:113 | ||||
| chr14:35808683-35808728 | Rare:15 | ||||
| chr14:35808802-35809006 | Common:1; Rare:55 | ||||
| chr14:35809160-35809336 | Common:1; Rare:47 | ||||
| chr14:35826137-35826534 | Common:1; Rare:108 | ||||
| chr14:35826633-35826960 | Common:1; Rare:104 | ||||
| chr14:36320140-36320185 | Rare:3 | ||||
| chr14:36320214-36320253 | Rare:8 | ||||
| chr14:36320297-36320360 | Rare:11 |