| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113410280-113410744 | Common:4; Rare:146 | ||||
| chr9:113593883-113594184 | Common:6; Rare:119 | ||||
| chr9:114587593-114587921 | Common:2; Rare:122 | ||||
| chr9:115055848-115055993 | Common:1; Rare:26 | ||||
| chr9:115073340-115073625 | Common:2; Rare:52 | ||||
| chr9:115118001-115118302 | Common:3; Rare:70 | ||||
| chr9:116153484-116153554 | Rare:9 | ||||
| chr9:116153560-116153972 | Common:2; Rare:102 | ||||
| chr9:116687221-116687376 | Common:3; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120793361-120793551 | Common:2; Rare:76 | ||||
| chr9:120842776-120843111 | Common:3; Rare:131 | ||||
| chr9:120877108-120877505 | Common:3; Rare:129 | ||||
| chr9:121074852-121074967 | Rare:56 | ||||
| chr9:121201849-121202188 | Common:2; Rare:92 | ||||
| chr9:121370192-121370520 | Common:2; Rare:99 |