| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111599785-111600025 | Common:2; Rare:59 | ||||
| chr9:111661385-111661673 | Common:3; Rare:78 | ||||
| chr9:112379768-112380157 | Common:4; Rare:148 | ||||
| chr9:113056657-113056840 | Common:1; Rare:65; Clinvar:1 | ||||
| chr9:113221230-113221594 | Common:1; Rare:118 | ||||
| chr9:113275359-113275734 | Common:5; Rare:119; Clinvar (pathogenic):1 | ||||
| chr9:113340237-113340431 | Common:3; Rare:49 | ||||
| chr9:113376914-113377108 | Common:7; Rare:64 | ||||
| chr9:113410226-113410754 | Common:4; Rare:165 | ||||
| chr9:114505501-114505644 | Rare:36 | ||||
| chr9:114587444-114587867 | Common:4; Rare:151 | ||||
| chr9:115036190-115036487 | Rare:67 | ||||
| chr9:115118001-115118245 | Common:3; Rare:56 | ||||
| chr9:115118247-115118454 | Rare:49 | ||||
| chr9:116687207-116687364 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):1 |