| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73027018-73027220 | Common:1; Rare:51 | ||||
| chr14:73058309-73058640 | Common:3; Rare:99 | ||||
| chr14:73458251-73458364 | Rare:22 | ||||
| chr14:73458491-73458870 | Common:5; Rare:102 | ||||
| chr14:73568866-73569090 | Common:1; Rare:31 | ||||
| chr14:73569136-73569298 | Rare:43 | ||||
| chr14:73592086-73592167 | Common:1; Rare:32 | ||||
| chr14:73644900-73645042 | Common:2; Rare:39; Clinvar:2 | ||||
| chr14:73714348-73714462 | Common:1; Rare:43 | ||||
| chr14:73787116-73787379 | Common:2; Rare:92 | ||||
| chr14:73790065-73790375 | Common:2; Rare:51 | ||||
| chr14:73851592-73852016 | Common:6; Rare:119 | ||||
| chr14:73886785-73886893 | Common:2; Rare:36 | ||||
| chr14:73950054-73950351 | Common:6; Rare:136; Clinvar (benign):4 | ||||
| chr14:74019201-74019468 | Common:2; Rare:102 |