| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26844076-26844220 | Common:1; Rare:38 | ||||
| chr9:26928103-26928405 | Rare:87 | ||||
| chr9:29213945-29214419 | Common:4; Rare:123 | ||||
| chr9:32550837-32551124 | Common:1; Rare:119; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:32964487-32964580 | Common:1; Rare:14 | ||||
| chr9:33818803-33818880 | Rare:12 | ||||
| chr9:34001986-34002295 | Common:2; Rare:59 | ||||
| chr9:35604026-35604360 | Common:3; Rare:92 | ||||
| chr9:35697691-35698170 | Rare:105 | ||||
| chr9:35699973-35700202 | Common:1; Rare:73 | ||||
| chr9:35725223-35725597 | Common:1; Rare:76 | ||||
| chr9:35733210-35733467 | Rare:93 | ||||
| chr9:35734841-35735212 | Common:2; Rare:102 | ||||
| chr9:36163893-36163960 | Common:4; Rare:6 | ||||
| chr9:37079800-37080039 | Common:4; Rare:79 |