| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30617311-30618139 | Common:1; Rare:249 | ||||
| chr13:31161832-31162050 | Rare:102 | ||||
| chr13:31162321-31162611 | Common:2; Rare:85 | ||||
| chr13:31199652-31199787 | Rare:31 | ||||
| chr13:31199835-31200070 | Common:1; Rare:93 | ||||
| chr13:31200208-31200419 | Common:2; Rare:59 | ||||
| chr13:32031007-32031174 | Common:1; Rare:35 | ||||
| chr13:32031224-32031373 | Common:1; Rare:43 | ||||
| chr13:32031497-32031797 | Common:1; Rare:79 | ||||
| chr13:32262371-32262456 | Rare:19 | ||||
| chr13:32314976-32315183 | Rare:32 | ||||
| chr13:32315284-32315607 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32315669-32315825 | Rare:37; Clinvar:1 | ||||
| chr13:32315852-32316012 | Common:2; Rare:35; Clinvar (benign):2 | ||||
| chr13:32316086-32316236 | Common:1; Rare:39; Clinvar (benign):1 |