| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:70359518-70359795 | Common:1; Rare:69 | ||||
| chr14:70416994-70417146 | Rare:46 | ||||
| chr14:70600633-70600987 | Common:3; Rare:83 | ||||
| chr14:71320296-71320491 | Rare:62 | ||||
| chr14:71320828-71321164 | Common:3; Rare:106 | ||||
| chr14:71586140-71586407 | Common:4; Rare:45 | ||||
| chr14:72926164-72926533 | Common:6; Rare:92 | ||||
| chr14:73058301-73058656 | Common:3; Rare:107 | ||||
| chr14:73136361-73136550 | Common:4; Rare:67; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:73458504-73458857 | Common:5; Rare:92 | ||||
| chr14:73568112-73568129 | Rare:2 | ||||
| chr14:73644900-73645042 | Common:2; Rare:39; Clinvar:2 | ||||
| chr14:73713791-73714016 | Rare:60 | ||||
| chr14:73714353-73714513 | Common:1; Rare:58 | ||||
| chr14:73886746-73886905 | Common:2; Rare:57 |