| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:108934074-108934477 | Common:7; Rare:161; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110579138-110579299 | Rare:46 | ||||
| chr9:110579551-110579659 | Common:1; Rare:31 | ||||
| chr9:111631137-111631372 | Common:1; Rare:65 | ||||
| chr9:112379824-112380146 | Common:3; Rare:130 | ||||
| chr9:113221242-113221597 | Common:1; Rare:114 | ||||
| chr9:113275392-113275678 | Common:4; Rare:80; Clinvar (pathogenic):1 | ||||
| chr9:113340240-113340513 | Common:5; Rare:65 | ||||
| chr9:116687228-116687375 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120793374-120793534 | Rare:59 | ||||
| chr9:120842917-120843111 | Common:1; Rare:65 | ||||
| chr9:120877186-120877516 | Common:1; Rare:114 | ||||
| chr9:121201862-121202179 | Common:2; Rare:83 | ||||
| chr9:121370189-121370508 | Common:2; Rare:98 | ||||
| chr9:122264801-122264919 | Common:1; Rare:33 |