| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113056657-113056883 | Common:1; Rare:76; Clinvar:1 | ||||
| chr9:113221235-113221628 | Common:1; Rare:125 | ||||
| chr9:113275392-113275746 | Common:5; Rare:119; Clinvar (pathogenic):1 | ||||
| chr9:113303081-113303272 | Rare:29 | ||||
| chr9:113376914-113377150 | Common:8; Rare:75 | ||||
| chr9:113401241-113401586 | Common:6; Rare:121; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410281-113410705 | Common:3; Rare:125 | ||||
| chr9:113463594-113463771 | Common:1; Rare:59 | ||||
| chr9:114098390-114098458 | Rare:25 | ||||
| chr9:114099234-114099454 | Common:1; Rare:50 | ||||
| chr9:114388013-114388170 | Common:1; Rare:50 | ||||
| chr9:115117985-115118284 | Common:3; Rare:69 | ||||
| chr9:116687228-116687364 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793242-120793543 | Common:2; Rare:110 | ||||
| chr9:120842890-120843139 | Common:1; Rare:94 |