| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30906025-30906280 | Common:3; Rare:51 | ||||
| chr13:30906604-30906793 | Common:1; Rare:56 | ||||
| chr13:31161635-31162214 | Common:2; Rare:248 | ||||
| chr13:32315345-32315553 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32315792-32316082 | Common:3; Rare:62; Clinvar (benign):4 | ||||
| chr13:32428097-32428392 | Rare:56 | ||||
| chr13:32586220-32586582 | Common:2; Rare:108 | ||||
| chr13:33205970-33206162 | Rare:36 | ||||
| chr13:33285651-33285887 | Rare:56 | ||||
| chr13:36131328-36131486 | Rare:37 | ||||
| chr13:36345505-36345783 | Common:1; Rare:64 | ||||
| chr13:36346249-36346477 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:36346616-36346841 | Common:4; Rare:65 | ||||
| chr13:36370238-36370277 | Rare:10 | ||||
| chr13:36999275-36999459 | Rare:74 |