| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:116687198-116687638 | Common:6; Rare:113; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120793353-120793535 | Common:1; Rare:75 | ||||
| chr9:120842905-120843137 | Common:1; Rare:85 | ||||
| chr9:121074850-121074967 | Rare:56 | ||||
| chr9:121201827-121202162 | Common:2; Rare:99 | ||||
| chr9:121370163-121370517 | Common:2; Rare:105 | ||||
| chr9:122264734-122264923 | Common:2; Rare:54 | ||||
| chr9:122905199-122905418 | Common:1; Rare:98 | ||||
| chr9:122931464-122931723 | Common:3; Rare:56 | ||||
| chr9:124940956-124941156 | Common:3; Rare:71 | ||||
| chr9:125189733-125190029 | Common:1; Rare:139 | ||||
| chr9:125240790-125241187 | Rare:121 | ||||
| chr9:125241275-125241656 | Common:2; Rare:114 | ||||
| chr9:125261728-125261925 | Common:2; Rare:66 | ||||
| chr9:126326989-126327005 | Rare:3 |