| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39458834-39459122 | Common:3; Rare:159; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527323-39527750 | Common:4; Rare:107 | ||||
| chr4:39638855-39639140 | Common:1; Rare:107 | ||||
| chr4:39697936-39698185 | Common:2; Rare:108 | ||||
| chr4:40056645-40056965 | Common:4; Rare:98 | ||||
| chr4:41360638-41360819 | Common:2; Rare:53 | ||||
| chr4:41538135-41538314 | Common:3; Rare:29 | ||||
| chr4:41612459-41613059 | Common:2; Rare:128 | ||||
| chr4:41934935-41935187 | Common:3; Rare:62 | ||||
| chr4:41990412-41990572 | Common:1; Rare:59 | ||||
| chr4:44678371-44678750 | Common:1; Rare:143 | ||||
| chr4:44726512-44726664 | Rare:60 | ||||
| chr4:47463648-47463802 | Common:2; Rare:50 | ||||
| chr4:47914569-47914853 | Common:1; Rare:89 | ||||
| chr4:48341108-48341581 | Common:2; Rare:189 |