| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:120793242-120793534 | Common:1; Rare:105 | ||||
| chr9:120842906-120843111 | Common:1; Rare:73 | ||||
| chr9:120868841-120869055 | Common:2; Rare:45 | ||||
| chr9:120877118-120877482 | Common:3; Rare:113 | ||||
| chr9:121074842-121074984 | Rare:71 | ||||
| chr9:121075109-121075202 | Rare:27 | ||||
| chr9:121201824-121202179 | Common:2; Rare:106 | ||||
| chr9:121268053-121268203 | Common:1; Rare:51 | ||||
| chr9:121281664-121281892 | Rare:62 | ||||
| chr9:121328609-121328919 | Common:3; Rare:81; Clinvar (benign):1 | ||||
| chr9:121370172-121370536 | Common:2; Rare:106 | ||||
| chr9:121566879-121567182 | Rare:80 | ||||
| chr9:122159702-122159938 | Rare:91 | ||||
| chr9:122264762-122264927 | Common:2; Rare:49 | ||||
| chr9:122931482-122931689 | Common:3; Rare:41 |