| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75276860-75277330 | Common:1; Rare:149 | ||||
| chr14:75294085-75294405 | Common:2; Rare:79 | ||||
| chr14:75298595-75299260 | Common:2; Rare:159 | ||||
| chr14:75981916-75982139 | Common:3; Rare:57 | ||||
| chr14:76904940-76905370 | Common:9; Rare:118 | ||||
| chr14:76953260-76953680 | Common:7; Rare:145 | ||||
| chr14:76956370-76956670 | Common:6; Rare:62 | ||||
| chr14:76959290-76959600 | Common:5; Rare:119 | ||||
| chr14:76961710-76962290 | Common:6; Rare:216 | ||||
| chr14:77025880-77026440 | Rare:350 | ||||
| chr14:77027000-77027712 | Common:35; Rare:500; Clinvar (pathogenic):1 | ||||
| chr14:77027802-77028044 | Rare:210 | ||||
| chr14:77033219-77033529 | Common:15; Rare:125 | ||||
| chr14:77033990-77034380 | Rare:97 | ||||
| chr14:77040144-77040850 | Common:2; Rare:240 |