| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113600612-113600741 | Rare:14 | ||||
| chr9:113620595-113620782 | Common:2; Rare:37 | ||||
| chr9:114114463-114114580 | Common:2; Rare:19 | ||||
| chr9:114138651-114138844 | Common:1; Rare:41 | ||||
| chr9:114385579-114385865 | Common:2; Rare:57 | ||||
| chr9:114387234-114387314 | Rare:18 | ||||
| chr9:114398452-114398678 | Common:2; Rare:59 | ||||
| chr9:114588964-114589147 | Rare:42 | ||||
| chr9:116155516-116155686 | Common:1; Rare:35 | ||||
| chr9:120475427-120475780 | Rare:61 | ||||
| chr9:120530045-120530243 | Rare:47; Clinvar:2 | ||||
| chr9:121303401-121303631 | Rare:43 | ||||
| chr9:121313817-121314023 | Rare:70; Clinvar:1 | ||||
| chr9:121316845-121317218 | Rare:103; Clinvar:1 | ||||
| chr9:121318392-121318907 | Common:1; Rare:149; Clinvar:2; Clinvar (benign):2 |