| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102868854-102869083 | Common:2; Rare:79 | ||||
| chr4:105708636-105708889 | Common:3; Rare:81 | ||||
| chr4:106316173-106316601 | Common:5; Rare:136 | ||||
| chr4:107035374-107035633 | Common:1; Rare:94 | ||||
| chr4:107036251-107036562 | Common:2; Rare:72 | ||||
| chr4:107283656-107283825 | Rare:34 | ||||
| chr4:107720151-107720519 | Common:8; Rare:151 | ||||
| chr4:107824328-107824736 | Common:1; Rare:79 | ||||
| chr4:107824753-107825031 | Common:1; Rare:71 | ||||
| chr4:107989689-107989928 | Common:5; Rare:110; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108168723-108168769 | Rare:7 | ||||
| chr4:108620462-108620699 | Common:4; Rare:111 | ||||
| chr4:108621646-108622004 | Common:2; Rare:75 | ||||
| chr4:109302713-109303022 | Common:4; Rare:86 | ||||
| chr4:109433755-109433942 | Common:1; Rare:62 |