| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143816773-143816970 | Common:1; Rare:69 | ||||
| chr8:143838681-143838872 | Rare:60 | ||||
| chr8:143935111-143935316 | Common:1; Rare:77; Clinvar:5; Clinvar (benign):4 | ||||
| chr8:143937168-143937583 | Common:1; Rare:130; Clinvar:2; Clinvar (benign):2 | ||||
| chr8:144700479-144700668 | Common:3; Rare:41 | ||||
| chr8:145002840-145003043 | Common:2; Rare:68 | ||||
| chr9:73853-74158 | Common:4; Rare:125 | ||||
| chr9:741983-742268 | Common:1; Rare:106 | ||||
| chr9:2191052-2191324 | Common:5; Rare:87; Clinvar (benign):2 | ||||
| chr9:2279201-2279492 | Common:12; Rare:80 | ||||
| chr9:4576974-4576996 | Rare:2 | ||||
| chr9:4579827-4580084 | Rare:52 | ||||
| chr9:4585145-4585387 | Rare:75; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr9:4688422-4688595 | Common:2; Rare:39 | ||||
| chr9:5629725-5629936 | Rare:51 |