| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102827906-102828301 | Common:3; Rare:131 | ||||
| chr4:102868850-102869046 | Common:2; Rare:63 | ||||
| chr4:105552324-105552617 | Rare:43 | ||||
| chr4:105708641-105708887 | Common:3; Rare:78 | ||||
| chr4:105895998-105896075 | Common:2; Rare:19 | ||||
| chr4:106316155-106316601 | Common:5; Rare:145 | ||||
| chr4:107720129-107720516 | Common:9; Rare:156 | ||||
| chr4:107824480-107824740 | Common:1; Rare:52 | ||||
| chr4:107824778-107825029 | Common:1; Rare:67 | ||||
| chr4:107989663-107989961 | Common:6; Rare:126; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108168814-108168930 | Common:1; Rare:27 | ||||
| chr4:108620367-108620717 | Common:6; Rare:158 | ||||
| chr4:109433757-109433972 | Common:1; Rare:71 | ||||
| chr4:109815300-109815798 | Common:3; Rare:125 | ||||
| chr4:110198500-110198643 | Rare:40 |