| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39366292-39366410 | Common:1; Rare:34 | ||||
| chr4:39458857-39459121 | Common:3; Rare:153; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527383-39527780 | Common:2; Rare:106 | ||||
| chr4:39527925-39528029 | Rare:24 | ||||
| chr4:39638703-39639209 | Common:1; Rare:172 | ||||
| chr4:39697930-39698185 | Common:2; Rare:111 | ||||
| chr4:39698338-39698366 | Rare:3 | ||||
| chr4:39977316-39977648 | Common:2; Rare:98 | ||||
| chr4:40056604-40056950 | Common:4; Rare:104 | ||||
| chr4:40629457-40629932 | Common:2; Rare:103 | ||||
| chr4:40630001-40630076 | Rare:17 | ||||
| chr4:40630130-40630182 | Common:1; Rare:6 | ||||
| chr4:40630571-40630808 | Common:2; Rare:50 | ||||
| chr4:41256719-41257019 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:41360699-41360859 | Common:1; Rare:48 |