| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113150643-113151053 | Common:6; Rare:101 | ||||
| chr9:113188016-113188176 | Common:2; Rare:19 | ||||
| chr9:113221222-113221602 | Common:1; Rare:123 | ||||
| chr9:113275392-113275708 | Common:5; Rare:99; Clinvar (pathogenic):1 | ||||
| chr9:113410308-113410715 | Common:3; Rare:118 | ||||
| chr9:113593846-113594160 | Common:4; Rare:119 | ||||
| chr9:116687251-116687376 | Common:1; Rare:38; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120793361-120793534 | Common:1; Rare:68 | ||||
| chr9:120842898-120843208 | Common:1; Rare:105 | ||||
| chr9:121201850-121202159 | Common:2; Rare:85 | ||||
| chr9:121370197-121370515 | Common:2; Rare:95 | ||||
| chr9:122264734-122264922 | Common:2; Rare:54 | ||||
| chr9:122931482-122931687 | Common:3; Rare:41 | ||||
| chr9:124861870-124862130 | Common:1; Rare:114 | ||||
| chr9:125189733-125190039 | Common:1; Rare:140 |