| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:52314191-52314319 | Rare:43 | ||||
| chr14:52552481-52552810 | Common:1; Rare:102 | ||||
| chr14:52707052-52707247 | Common:1; Rare:85 | ||||
| chr14:52729832-52730237 | Common:2; Rare:124 | ||||
| chr14:52791397-52791799 | Common:2; Rare:126 | ||||
| chr14:52951009-52951439 | Common:4; Rare:152 | ||||
| chr14:53152364-53152465 | Rare:40 | ||||
| chr14:53152614-53153064 | Common:9; Rare:197; Clinvar:2; Clinvar (benign):10 | ||||
| chr14:53153212-53153417 | Common:2; Rare:82 | ||||
| chr14:54396740-54397071 | Common:2; Rare:95 | ||||
| chr14:54488830-54489164 | Common:3; Rare:96 | ||||
| chr14:54509668-54509997 | Common:5; Rare:119 | ||||
| chr14:54567024-54567240 | Rare:59 | ||||
| chr14:54687808-54688094 | Rare:48 | ||||
| chr14:54754718-54754818 | Rare:20 |