| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46211740-46212141 | Common:2; Rare:103 | ||||
| chr13:46553023-46553193 | Common:2; Rare:61 | ||||
| chr13:46797098-46797315 | Common:3; Rare:76 | ||||
| chr13:48001235-48001434 | Common:1; Rare:92; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037388-48037798 | Common:3; Rare:159 | ||||
| chr13:48037920-48038019 | Common:3; Rare:37 | ||||
| chr13:48095058-48095206 | Rare:70 | ||||
| chr13:48233089-48233183 | Rare:20 | ||||
| chr13:48303665-48303906 | Rare:82; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48533050-48533140 | Common:1; Rare:30 | ||||
| chr13:48975764-48975960 | Common:2; Rare:67 | ||||
| chr13:48976161-48976252 | Rare:25 | ||||
| chr13:48976426-48976846 | Common:3; Rare:129 | ||||
| chr13:49110243-49110386 | Common:1; Rare:39 | ||||
| chr13:49247823-49247976 | Rare:48 |