| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:76885505-76885826 | Not yet | Common:1; Rare:115 | 204 | ||
| chr13:95083823-95084097 | Not yet | Common:3; Rare:34 | 381 | ||
| chr13:98976028-98976162 | Not yet | Common:1; Rare:26 | 241 | ||
| chr13:98992502-98992691 | Not yet | Rare:48 | 345 | ||
| chr13:110205351-110205532 | Not yet | Common:1; Rare:72; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | 255 | ||
| chr13:110212415-110212574 | Not yet | Common:1; Rare:51; Clinvar (benign):1 | 269 | ||
| chr13:110307826-110308123 | Not yet | Common:1; Rare:111 | 293 | ||
| chr13:110308515-110308622 | Not yet | Common:1; Rare:21 | 181 | ||
| chr13:110409539-110409829 | Not yet | Common:3; Rare:46 | 399 | ||
| chr13:110870188-110870566 | Not yet | Common:3; Rare:57 | 414 | ||
| chr14:33564779-33565040 | Not yet | Common:1; Rare:57 | 408 | ||
| chr14:38254565-38254912 | Not yet | Rare:118 | 346 | ||
| chr14:49633949-49634110 | Not yet | Common:1; Rare:77; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | 132 | ||
| chr14:49862645-49862948 | Not yet | Common:1; Rare:150 | 338 | ||
| chr14:61751057-61751219 | Not yet | Rare:40 | 209 |