| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:110125345-110125576 | Rare:45 | ||||
| chr9:111661509-111661666 | Common:3; Rare:48 | ||||
| chr9:112333565-112333949 | Rare:122 | ||||
| chr9:112379800-112380146 | Common:3; Rare:140 | ||||
| chr9:113150868-113151040 | Rare:57 | ||||
| chr9:113221235-113221633 | Common:1; Rare:128 | ||||
| chr9:113275376-113275734 | Common:5; Rare:114; Clinvar (pathogenic):1 | ||||
| chr9:113410645-113410857 | Common:2; Rare:69 | ||||
| chr9:113565347-113565598 | Common:1; Rare:59 | ||||
| chr9:113593863-113594184 | Common:6; Rare:123 | ||||
| chr9:114587387-114587893 | Common:4; Rare:170 | ||||
| chr9:115118111-115118459 | Rare:83 | ||||
| chr9:116153565-116153922 | Common:2; Rare:87 | ||||
| chr9:116687207-116687370 | Common:3; Rare:60; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120793248-120793534 | Common:1; Rare:104 |