| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:94596132-94596348 | Common:2; Rare:70 | ||||
| chr13:94601596-94601945 | Common:3; Rare:111 | ||||
| chr13:95676918-95677197 | Common:3; Rare:100 | ||||
| chr13:96053232-96053488 | Common:2; Rare:107 | ||||
| chr13:97222197-97222511 | Rare:55 | ||||
| chr13:98576183-98576329 | Common:1; Rare:51 | ||||
| chr13:99200668-99200911 | Common:6; Rare:116 | ||||
| chr13:99307337-99307447 | Rare:15 | ||||
| chr13:99307469-99307739 | Common:4; Rare:43 | ||||
| chr13:100088914-100089147 | Rare:90; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr13:102596760-102597082 | Common:1; Rare:135; Clinvar (benign):1 | ||||
| chr13:102773716-102773868 | Rare:63 | ||||
| chr13:106568069-106568267 | Rare:61 | ||||
| chr13:107867071-107867151 | Rare:20 | ||||
| chr13:108218313-108218525 | Rare:80 |