| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:23579247-23579419 | Common:2; Rare:53 | ||||
| chr13:23889306-23889465 | Rare:55 | ||||
| chr13:24160528-24160764 | Rare:69 | ||||
| chr13:24512739-24512856 | Common:3; Rare:34 | ||||
| chr13:26221791-26221923 | Rare:33 | ||||
| chr13:27251245-27251609 | Common:5; Rare:110 | ||||
| chr13:27270730-27270831 | Rare:30 | ||||
| chr13:27450037-27450222 | Common:3; Rare:57 | ||||
| chr13:27450526-27450621 | Common:2; Rare:43 | ||||
| chr13:27620461-27620810 | Common:2; Rare:119 | ||||
| chr13:28137969-28138222 | Common:3; Rare:68 | ||||
| chr13:28659076-28659194 | Rare:52; Clinvar (pathogenic):1 | ||||
| chr13:30306840-30307207 | Common:6; Rare:101 | ||||
| chr13:30307377-30307546 | Common:2; Rare:60 | ||||
| chr13:30465760-30466087 | Common:1; Rare:107 |