| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37890995-37891238 | Common:2; Rare:75 | ||||
| chr4:38664211-38664312 | Rare:33 | ||||
| chr4:38867682-38867830 | Common:1; Rare:59 | ||||
| chr4:39366315-39366416 | Rare:30 | ||||
| chr4:39458868-39459112 | Common:3; Rare:136; Clinvar (benign):5 | ||||
| chr4:39527282-39527761 | Common:6; Rare:122 | ||||
| chr4:39527952-39528047 | Rare:26 | ||||
| chr4:39638816-39639140 | Common:1; Rare:116 | ||||
| chr4:39697771-39698185 | Common:2; Rare:141 | ||||
| chr4:41990389-41990661 | Common:2; Rare:96 | ||||
| chr4:44678352-44678706 | Common:1; Rare:130 | ||||
| chr4:44726481-44726633 | Common:2; Rare:54 | ||||
| chr4:47485219-47485408 | Common:2; Rare:60 | ||||
| chr4:47578023-47578153 | Common:1; Rare:18 | ||||
| chr4:48016638-48016774 | Common:1; Rare:37 |