| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:105708584-105708877 | Common:3; Rare:96 | ||||
| chr4:106315231-106315586 | Common:3; Rare:71 | ||||
| chr4:106315886-106315941 | Rare:12 | ||||
| chr4:106315945-106316050 | Common:1; Rare:24 | ||||
| chr4:106316135-106316683 | Common:5; Rare:171 | ||||
| chr4:107719846-107719893 | Common:2; Rare:15 | ||||
| chr4:107719896-107720036 | Common:2; Rare:38 | ||||
| chr4:107720083-107720500 | Common:9; Rare:168 | ||||
| chr4:107989679-107989942 | Common:6; Rare:117; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620350-108620717 | Common:6; Rare:164 | ||||
| chr4:109302655-109302774 | Common:2; Rare:41 | ||||
| chr4:109433473-109433694 | Common:1; Rare:68 | ||||
| chr4:109433750-109433926 | Common:1; Rare:59 | ||||
| chr4:109815452-109815818 | Common:1; Rare:95 | ||||
| chr4:110198484-110198619 | Rare:36 |