| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:121286059-121286140 | Rare:19 | ||||
| chr9:121299712-121300004 | Common:2; Rare:102; Clinvar:3 | ||||
| chr9:121326157-121326790 | Common:7; Rare:173; Clinvar:3; Clinvar (benign):5 | ||||
| chr9:121328885-121329315 | Common:1; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:121370126-121370512 | Common:2; Rare:114 | ||||
| chr9:122159661-122159933 | Rare:115 | ||||
| chr9:122264535-122264696 | Common:2; Rare:37 | ||||
| chr9:122264742-122264933 | Common:2; Rare:58 | ||||
| chr9:122828474-122828832 | Rare:101 | ||||
| chr9:122905044-122905417 | Common:1; Rare:137 | ||||
| chr9:122913268-122913431 | Common:3; Rare:36 | ||||
| chr9:122931248-122931344 | Rare:18 | ||||
| chr9:122931464-122931724 | Common:3; Rare:56 | ||||
| chr9:122940818-122941092 | Common:2; Rare:109 | ||||
| chr9:122941239-122941352 | Rare:37 |