| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:39037779-39038456 | Common:2; Rare:186 | ||||
| chr13:39655583-39655816 | Common:4; Rare:117; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40666578-40666805 | Common:2; Rare:84 | ||||
| chr13:40771006-40771444 | Common:3; Rare:143 | ||||
| chr13:40789326-40789644 | Common:2; Rare:111; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:41060838-41061024 | Common:16; Rare:119 | ||||
| chr13:41061352-41061674 | Common:2; Rare:101 | ||||
| chr13:41132692-41133038 | Common:1; Rare:87 | ||||
| chr13:41194426-41194618 | Common:2; Rare:42 | ||||
| chr13:41311093-41311341 | Common:1; Rare:100 | ||||
| chr13:41961022-41961131 | Common:2; Rare:37 | ||||
| chr13:42040416-42040621 | Common:1; Rare:69 | ||||
| chr13:42271929-42272193 | Common:2; Rare:59 | ||||
| chr13:42574588-42574664 | Common:1; Rare:15 | ||||
| chr13:43879482-43879920 | Common:19; Rare:116 |