| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48413064-48413208 | Not yet | Rare:20 | 194 | ||
| chr13:52194408-52194542 | Not yet | Rare:37 | 192 | ||
| chr13:73497533-73497769 | Not yet | Rare:40 | 370 | ||
| chr13:73611104-73611188 | Not yet | Rare:14 | 202 | ||
| chr13:109148297-109148550 | Not yet | Common:1; Rare:47 | 352 | ||
| chr13:109265126-109265419 | Not yet | Common:4; Rare:68 | 415 | ||
| chr13:109272007-109272217 | Not yet | Common:6; Rare:46 | 340 | ||
| chr14:22980676-22980894 | Not yet | Common:1; Rare:48 | 190 | ||
| chr14:49633956-49634064 | Not yet | Common:1; Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | 98 | ||
| chr14:49862651-49863044 | Not yet | Common:1; Rare:181 | 377 | ||
| chr14:51397173-51397335 | Not yet | Common:1; Rare:41 | 232 | ||
| chr14:68547614-68547815 | Not yet | Common:1; Rare:25 | 265 | ||
| chr14:70698439-70698609 | Not yet | Common:2; Rare:19 | 278 | ||
| chr14:73246009-73246106 | Not yet | Rare:40 | 134 | ||
| chr14:75222113-75222372 | Not yet | Common:2; Rare:48 | 353 |