| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48001222-48001397 | Common:1; Rare:82; Clinvar:3; Clinvar (benign):7 | ||||
| chr13:48037628-48037789 | Common:1; Rare:74 | ||||
| chr13:48037929-48038096 | Common:5; Rare:54 | ||||
| chr13:48094987-48095030 | Rare:18 | ||||
| chr13:48095039-48095317 | Common:2; Rare:125 | ||||
| chr13:48233383-48233473 | Common:2; Rare:35 | ||||
| chr13:48303692-48304032 | Common:1; Rare:107; Clinvar:15; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr13:48975811-48975929 | Rare:44 | ||||
| chr13:49110262-49110397 | Common:1; Rare:39 | ||||
| chr13:49247807-49247982 | Rare:50 | ||||
| chr13:49443951-49444457 | Common:1; Rare:156 | ||||
| chr13:49495853-49496079 | Rare:55 | ||||
| chr13:49585459-49585628 | Common:1; Rare:54 | ||||
| chr13:49691255-49691290 | Rare:8 | ||||
| chr13:49691350-49691528 | Common:2; Rare:73 |