| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99563668-99563791 | Rare:31 | ||||
| chr4:99563983-99564127 | Common:2; Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:99894333-99894620 | Common:3; Rare:98 | ||||
| chr4:99946569-99946846 | Rare:96 | ||||
| chr4:101347527-101347816 | Common:5; Rare:91 | ||||
| chr4:102760920-102761067 | Rare:53; Clinvar:1 | ||||
| chr4:102826779-102826987 | Rare:62 | ||||
| chr4:102827120-102827421 | Common:1; Rare:109 | ||||
| chr4:102827439-102827666 | Common:1; Rare:84 | ||||
| chr4:102827691-102828299 | Common:6; Rare:191 | ||||
| chr4:102868836-102869083 | Common:2; Rare:88 | ||||
| chr4:103198339-103198499 | Common:2; Rare:41 | ||||
| chr4:104494879-104495135 | Common:2; Rare:53 | ||||
| chr4:105708636-105708873 | Common:2; Rare:79 | ||||
| chr4:105895292-105895539 | Rare:75 |