| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:40771005-40771425 | Common:4; Rare:190 | ||||
| chr13:40789255-40789920 | Common:10; Rare:483; Clinvar:18; Clinvar (benign):6 | ||||
| chr13:41019225-41019450 | Rare:73 | ||||
| chr13:41060081-41060594 | Common:9; Rare:460 | ||||
| chr13:41061002-41061558 | Common:6; Rare:306 | ||||
| chr13:41061479-41061974 | Common:4; Rare:247 | ||||
| chr13:41132695-41133058 | Common:2; Rare:247 | ||||
| chr13:41194344-41194760 | Common:4; Rare:145 | ||||
| chr13:41263460-41263638 | Rare:46 | ||||
| chr13:41311024-41311470 | Common:7; Rare:344 | ||||
| chr13:41457286-41457605 | Common:6; Rare:212 | ||||
| chr13:41960859-41961385 | Common:8; Rare:273 | ||||
| chr13:41961392-41961546 | Rare:18 | ||||
| chr13:42039972-42040176 | Common:4; Rare:87 | ||||
| chr13:42040271-42040784 | Common:5; Rare:332 |