| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30307372-30307596 | Common:2; Rare:77 | ||||
| chr13:30616981-30617140 | Rare:29 | ||||
| chr13:30617255-30617337 | Rare:15 | ||||
| chr13:30617340-30618034 | Common:1; Rare:222 | ||||
| chr13:30932626-30932709 | Rare:23 | ||||
| chr13:31162341-31162473 | Common:1; Rare:39 | ||||
| chr13:32031045-32031352 | Common:2; Rare:75 | ||||
| chr13:32586248-32586593 | Common:2; Rare:107 | ||||
| chr13:33285670-33285938 | Common:1; Rare:60 | ||||
| chr13:33817989-33818212 | Common:1; Rare:101 | ||||
| chr13:34942163-34942298 | Common:3; Rare:39 | ||||
| chr13:35476657-35476822 | Common:1; Rare:26 | ||||
| chr13:35855549-35855744 | Common:1; Rare:43 | ||||
| chr13:36297794-36297922 | Rare:48 | ||||
| chr13:36346282-36346454 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):1 |