| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:24922801-24923150 | Common:2; Rare:122; Clinvar:1 | ||||
| chr13:25301485-25301721 | Common:1; Rare:86 | ||||
| chr13:26221787-26221939 | Rare:39 | ||||
| chr13:27251235-27251617 | Common:8; Rare:117 | ||||
| chr13:27450531-27450643 | Common:2; Rare:47 | ||||
| chr13:27620440-27620828 | Common:2; Rare:129 | ||||
| chr13:28138147-28138224 | Common:1; Rare:19 | ||||
| chr13:28659066-28659180 | Rare:50; Clinvar (pathogenic):1 | ||||
| chr13:30306813-30307228 | Common:7; Rare:117 | ||||
| chr13:30307368-30307615 | Common:3; Rare:79 | ||||
| chr13:30617335-30618046 | Common:1; Rare:227 | ||||
| chr13:32031057-32031352 | Common:2; Rare:71 | ||||
| chr13:32031537-32031667 | Rare:26 | ||||
| chr13:32031684-32031816 | Common:1; Rare:43 | ||||
| chr13:32315429-32315542 | Rare:35; Clinvar:2; Clinvar (benign):1 |