| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:112889856-112890059 | Common:2; Rare:77 | ||||
| chr9:113173505-113173721 | Rare:46 | ||||
| chr9:113184770-113185041 | Rare:57 | ||||
| chr9:120851280-120851282 | |||||
| chr9:121316802-121317213 | Common:1; Rare:106; Clinvar:1 | ||||
| chr9:121318379-121318853 | Common:1; Rare:135; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:121324302-121324626 | Common:1; Rare:71 | ||||
| chr9:121332321-121332585 | Common:2; Rare:71; Clinvar (benign):2 | ||||
| chr9:121499662-121499827 | Rare:52 | ||||
| chr9:121736995-121737223 | Common:4; Rare:52 | ||||
| chr9:122369706-122369977 | Common:3; Rare:60 | ||||
| chr9:124353593-124353865 | Common:1; Rare:68 | ||||
| chr9:124658174-124658436 | Rare:46 | ||||
| chr9:127487602-127487679 | Rare:23 | ||||
| chr9:127493827-127494117 | Common:1; Rare:53 |