| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136712244-136712561 | Common:1; Rare:103 | ||||
| chr9:136807789-136808101 | Common:2; Rare:119 | ||||
| chr9:136866193-136866350 | Common:1; Rare:71 | ||||
| chr9:136886251-136886533 | Common:2; Rare:83 | ||||
| chr9:136944606-136944786 | Rare:75 | ||||
| chr9:137032394-137032607 | Common:1; Rare:49 | ||||
| chr9:137033027-137033211 | Common:2; Rare:68 | ||||
| chr9:137086720-137087102 | Common:1; Rare:148; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:137188544-137188734 | Common:2; Rare:94 | ||||
| chr9:137205602-137205753 | Rare:65 | ||||
| chr9:137423152-137423431 | Common:2; Rare:87 | ||||
| chr9:137550364-137550506 | Rare:22 | ||||
| chr9:137618803-137619035 | Common:1; Rare:104 | ||||
| chrM:3095-3252 | |||||
| chrM:3256-3447 |