| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113221225-113221625 | Common:1; Rare:127 | ||||
| chr9:113275348-113275734 | Common:5; Rare:124; Clinvar (pathogenic):1 | ||||
| chr9:113410308-113410488 | Common:1; Rare:64 | ||||
| chr9:113410595-113410791 | Common:3; Rare:63 | ||||
| chr9:113593866-113594209 | Common:6; Rare:141 | ||||
| chr9:114387950-114388104 | Common:1; Rare:50 | ||||
| chr9:114587413-114587846 | Common:4; Rare:151 | ||||
| chr9:114587869-114587923 | Rare:20 | ||||
| chr9:115063621-115063972 | Common:2; Rare:96; Clinvar:1 | ||||
| chr9:115117999-115118452 | Common:3; Rare:106 | ||||
| chr9:116153565-116153871 | Common:1; Rare:70 | ||||
| chr9:116154272-116154559 | Common:2; Rare:77 | ||||
| chr9:116687198-116687628 | Common:6; Rare:113; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120403193-120403388 | Rare:29 | ||||
| chr9:120793143-120793573 | Common:6; Rare:147 |