| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:95676912-95677197 | Common:3; Rare:102 | ||||
| chr13:96053321-96053465 | Common:1; Rare:67 | ||||
| chr13:98576218-98576329 | Common:1; Rare:39 | ||||
| chr13:99200662-99200911 | Common:6; Rare:117 | ||||
| chr13:99307375-99307706 | Common:3; Rare:47 | ||||
| chr13:99606514-99606698 | Common:5; Rare:54 | ||||
| chr13:100088901-100089167 | Rare:101; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:100674778-100675060 | Common:3; Rare:115 | ||||
| chr13:102596785-102597041 | Common:1; Rare:120 | ||||
| chr13:106567633-106567837 | Rare:62 | ||||
| chr13:106567841-106568267 | Rare:117 | ||||
| chr13:108218313-108218544 | Rare:84 | ||||
| chr13:110307155-110307465 | Common:5; Rare:97; Clinvar (benign):5 | ||||
| chr13:110561641-110561912 | Common:5; Rare:91 | ||||
| chr13:110615382-110615656 | Common:2; Rare:94 |