| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113221221-113221603 | Common:1; Rare:125 | ||||
| chr9:113275376-113275728 | Common:5; Rare:113; Clinvar (pathogenic):1 | ||||
| chr9:113410197-113410728 | Common:3; Rare:166 | ||||
| chr9:113501343-113501583 | Rare:60 | ||||
| chr9:113593870-113594210 | Common:6; Rare:141 | ||||
| chr9:114387967-114388121 | Common:1; Rare:50 | ||||
| chr9:114587453-114587914 | Common:4; Rare:168 | ||||
| chr9:116687211-116687370 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120793248-120793534 | Common:1; Rare:104 | ||||
| chr9:120842890-120843107 | Common:1; Rare:80 | ||||
| chr9:121074863-121074967 | Rare:47 | ||||
| chr9:121201820-121202158 | Common:2; Rare:104 | ||||
| chr9:121370213-121370483 | Common:1; Rare:76 | ||||
| chr9:121566868-121567191 | Rare:88 | ||||
| chr9:122159695-122159933 | Rare:95 |