| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111759512-111759525 | |||||
| chr9:111783862-111784072 | Common:3; Rare:28 | ||||
| chr9:111794904-111795071 | Common:2; Rare:50 | ||||
| chr9:112332848-112332898 | Rare:23 | ||||
| chr9:112332901-112333063 | Common:1; Rare:45 | ||||
| chr9:112333310-112333388 | Rare:21 | ||||
| chr9:112333473-112333930 | Rare:130 | ||||
| chr9:112379753-112380153 | Common:4; Rare:152 | ||||
| chr9:112413897-112414030 | Common:1; Rare:20 | ||||
| chr9:112718002-112718170 | Common:2; Rare:43 | ||||
| chr9:113056645-113056883 | Common:1; Rare:77; Clinvar:1 | ||||
| chr9:113150644-113151080 | Common:7; Rare:111 | ||||
| chr9:113221235-113221617 | Common:1; Rare:121 | ||||
| chr9:113275217-113275746 | Common:5; Rare:166; Clinvar (pathogenic):1 | ||||
| chr9:113303547-113303635 | Rare:15 |