| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27450036-27450232 | Common:3; Rare:59 | ||||
| chr13:27450518-27450643 | Common:2; Rare:54 | ||||
| chr13:27620429-27620810 | Common:2; Rare:128 | ||||
| chr13:28138117-28138229 | Common:1; Rare:38 | ||||
| chr13:28658948-28659202 | Rare:111; Clinvar (pathogenic):1 | ||||
| chr13:28718496-28718613 | Rare:19 | ||||
| chr13:28718787-28719123 | Common:1; Rare:86 | ||||
| chr13:30306813-30307204 | Common:7; Rare:105 | ||||
| chr13:30307330-30307604 | Common:2; Rare:83 | ||||
| chr13:30465767-30466064 | Common:1; Rare:98 | ||||
| chr13:30617294-30618234 | Common:1; Rare:272 | ||||
| chr13:30618425-30618741 | Common:2; Rare:64 | ||||
| chr13:32031311-32031453 | Rare:39 | ||||
| chr13:32031645-32031809 | Common:1; Rare:52 | ||||
| chr13:32428078-32428205 | Rare:29 |