| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:38349494-38349938 | Common:8; Rare:275; Clinvar (pathogenic):2 | ||||
| chr13:38350170-38350520 | Common:2; Rare:159 | ||||
| chr13:39037773-39038482 | Common:3; Rare:314 | ||||
| chr13:39655557-39655802 | Common:6; Rare:203; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr13:40666565-40666779 | Common:4; Rare:159 | ||||
| chr13:40771145-40771319 | Common:3; Rare:49 | ||||
| chr13:40789335-40789621 | Common:4; Rare:147; Clinvar:8; Clinvar (benign):4 | ||||
| chr13:41060800-41061280 | Common:35; Rare:425 | ||||
| chr13:41061349-41061597 | Common:4; Rare:148 | ||||
| chr13:41132723-41133032 | Common:1; Rare:144 | ||||
| chr13:41194465-41194685 | Common:4; Rare:83 | ||||
| chr13:41263740-41264030 | Common:1; Rare:55 | ||||
| chr13:41310916-41311354 | Common:3; Rare:200 | ||||
| chr13:41960868-41961142 | Common:2; Rare:86 | ||||
| chr13:41961057-41961186 | Common:2; Rare:48 |