| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73136197-73136614 | Common:9; Rare:223; Clinvar:8; Clinvar (benign):2 | ||||
| chr14:73136898-73137078 | Common:2; Rare:57 | ||||
| chr14:73457139-73457929 | Common:9; Rare:238 | ||||
| chr14:73458045-73458147 | Common:3; Rare:15 | ||||
| chr14:73458223-73458915 | Common:17; Rare:387 | ||||
| chr14:73490790-73491070 | Common:13; Rare:231 | ||||
| chr14:73491530-73491855 | Common:6; Rare:261 | ||||
| chr14:73568982-73569382 | Rare:242 | ||||
| chr14:73591791-73592242 | Common:9; Rare:356 | ||||
| chr14:73610709-73611004 | Common:2; Rare:37 | ||||
| chr14:73644803-73645066 | Common:9; Rare:172; Clinvar:6; Clinvar (benign):3 | ||||
| chr14:73713680-73714210 | Common:2; Rare:257 | ||||
| chr14:73714184-73714435 | Common:2; Rare:122 | ||||
| chr14:73755380-73755684 | Common:5; Rare:86 | ||||
| chr14:73759797-73760530 | Common:8; Rare:324 |