| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:39603040-39603550 | Common:2; Rare:156 | ||||
| chr13:39655530-39655765 | Common:4; Rare:121; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:40666567-40666768 | Common:2; Rare:81 | ||||
| chr13:40666986-40667151 | Rare:37 | ||||
| chr13:40771130-40771346 | Common:3; Rare:72 | ||||
| chr13:40789336-40789636 | Common:2; Rare:103; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:41060214-41060514 | Common:2; Rare:103 | ||||
| chr13:41061355-41061680 | Common:2; Rare:103 | ||||
| chr13:41061690-41061860 | Common:2; Rare:127 | ||||
| chr13:41132697-41133048 | Common:1; Rare:88 | ||||
| chr13:41194443-41194744 | Common:2; Rare:69 | ||||
| chr13:41263532-41263643 | Rare:26 | ||||
| chr13:41960884-41961246 | Common:3; Rare:114 | ||||
| chr13:41961330-41961432 | Rare:19 | ||||
| chr13:42039736-42040136 | Common:7; Rare:121 |