| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:116687140-116687380 | Common:8; Rare:166; Clinvar:4; Clinvar (benign):4 | ||||
| chr9:120536187-120536770 | Common:4; Rare:402; Clinvar:21; Clinvar (benign):6 | ||||
| chr9:120579991-120580393 | Common:3; Rare:214; Clinvar:10; Clinvar (benign):1 | ||||
| chr9:120714407-120714689 | Common:5; Rare:169 | ||||
| chr9:120793242-120793562 | Common:7; Rare:227 | ||||
| chr9:120842875-120843251 | Common:2; Rare:218 | ||||
| chr9:120876270-120876650 | Common:4; Rare:157 | ||||
| chr9:120877116-120877516 | Common:6; Rare:238 | ||||
| chr9:121050191-121050574 | Rare:86 | ||||
| chr9:121074848-121074975 | Rare:115 | ||||
| chr9:121075030-121075420 | Rare:180 | ||||
| chr9:121201784-121202187 | Common:4; Rare:230 | ||||
| chr9:121299690-121299972 | Common:1; Rare:134; Clinvar:4 | ||||
| chr9:121370145-121370670 | Common:6; Rare:258 | ||||
| chr9:122093272-122093465 | Common:1; Rare:83 |