| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111631156-111631369 | Common:1; Rare:56 | ||||
| chr9:111661486-111661666 | Common:3; Rare:51 | ||||
| chr9:111897189-111897248 | Rare:22 | ||||
| chr9:112379824-112380160 | Common:3; Rare:132 | ||||
| chr9:112718014-112718159 | Common:2; Rare:36 | ||||
| chr9:113056664-113056824 | Common:1; Rare:58; Clinvar:1 | ||||
| chr9:113221228-113221661 | Common:1; Rare:133 | ||||
| chr9:113275373-113275737 | Common:5; Rare:115; Clinvar (pathogenic):1 | ||||
| chr9:113410308-113410742 | Common:4; Rare:134 | ||||
| chr9:115117991-115118172 | Common:3; Rare:41 | ||||
| chr9:116687203-116687376 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120793263-120793543 | Common:2; Rare:104 | ||||
| chr9:120842782-120843215 | Common:3; Rare:156 | ||||
| chr9:120868823-120869127 | Common:2; Rare:69 | ||||
| chr9:121074879-121074969 | Rare:39 |