| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:26222250-26222339 | Common:2; Rare:24 | ||||
| chr13:27251235-27251608 | Common:7; Rare:114 | ||||
| chr13:27270696-27270858 | Rare:61 | ||||
| chr13:27450119-27450222 | Common:3; Rare:32 | ||||
| chr13:27450507-27450685 | Common:2; Rare:69 | ||||
| chr13:27620473-27620790 | Common:2; Rare:107 | ||||
| chr13:28138117-28138206 | Rare:29 | ||||
| chr13:28658948-28659194 | Rare:107; Clinvar (pathogenic):1 | ||||
| chr13:30306994-30307207 | Common:5; Rare:53 | ||||
| chr13:30465795-30466012 | Common:1; Rare:78 | ||||
| chr13:30617290-30618028 | Common:1; Rare:228 | ||||
| chr13:32315364-32315536 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:32538676-32538904 | Common:1; Rare:70 | ||||
| chr13:32586260-32586582 | Common:2; Rare:98 | ||||
| chr13:33206017-33206147 | Rare:28 |