| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:41990390-41990576 | Common:1; Rare:68 | ||||
| chr4:44678411-44678706 | Common:1; Rare:111 | ||||
| chr4:47485210-47485340 | Common:1; Rare:48 | ||||
| chr4:48341188-48341486 | Common:1; Rare:124 | ||||
| chr4:48780259-48780572 | Common:2; Rare:91 | ||||
| chr4:52659268-52659407 | Common:1; Rare:47 | ||||
| chr4:55395855-55395957 | Rare:27; Clinvar:2 | ||||
| chr4:56387423-56387528 | Rare:35 | ||||
| chr4:56435546-56435759 | Common:3; Rare:73 | ||||
| chr4:56467555-56467699 | Common:2; Rare:60; Clinvar (benign):5 | ||||
| chr4:67545442-67545741 | Common:2; Rare:75 | ||||
| chr4:67701124-67701358 | Common:4; Rare:109 | ||||
| chr4:68349975-68350209 | Common:1; Rare:85 | ||||
| chr4:69860094-69860285 | Common:1; Rare:34 | ||||
| chr4:70688382-70688567 | Common:2; Rare:52 |