| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:101445380-101445790 | Rare:139 | ||||
| chr9:104889536-104889943 | Common:2; Rare:127 | ||||
| chr9:104899874-104900017 | Rare:20 | ||||
| chr9:104903657-104903944 | Common:5; Rare:119; Clinvar (benign):8 | ||||
| chr9:104926360-104926790 | Common:25; Rare:196 | ||||
| chr9:105291470-105291720 | Common:1; Rare:25 | ||||
| chr9:105418520-105419010 | Common:2; Rare:108 | ||||
| chr9:108775940-108776360 | Common:2; Rare:119 | ||||
| chr9:108884826-108885022 | Common:2; Rare:60 | ||||
| chr9:108885760-108886260 | Common:3; Rare:128 | ||||
| chr9:109477530-109477850 | Common:2; Rare:126 | ||||
| chr9:112119452-112120001 | Common:2; Rare:140 | ||||
| chr9:112487580-112487910 | Common:2; Rare:104 | ||||
| chr9:113455370-113455660 | Common:2; Rare:85 | ||||
| chr9:113503855-113504038 | Common:2; Rare:83 |