| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:34785845-34786129 | Common:1; Rare:49 | ||||
| chr14:34982373-34982706 | Common:1; Rare:134 | ||||
| chr14:35046130-35046580 | Common:1; Rare:153 | ||||
| chr14:35122239-35122654 | Common:1; Rare:120 | ||||
| chr14:35292220-35292465 | Common:4; Rare:92 | ||||
| chr14:35404541-35404804 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):4 | ||||
| chr14:36320584-36320764 | Common:3; Rare:57 | ||||
| chr14:38256077-38256364 | Common:1; Rare:71 | ||||
| chr14:39174916-39175285 | Common:5; Rare:129 | ||||
| chr14:39432420-39432650 | Common:6; Rare:79 | ||||
| chr14:41608184-41608309 | Rare:28 | ||||
| chr14:44961892-44962261 | Common:3; Rare:106 | ||||
| chr14:45135731-45135979 | Common:1; Rare:47 | ||||
| chr14:45253065-45253316 | Rare:71 | ||||
| chr14:49586337-49586776 | Common:1; Rare:236 |