| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17810677-17811001 | Common:2; Rare:99 | ||||
| chr4:20700292-20700495 | Common:1; Rare:93 | ||||
| chr4:23890042-23890234 | Common:1; Rare:27 | ||||
| chr4:25160411-25160725 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25376991-25377325 | Common:3; Rare:100 | ||||
| chr4:25914051-25914297 | Common:2; Rare:103 | ||||
| chr4:26320939-26321041 | Rare:39 | ||||
| chr4:26583857-26584124 | Rare:57 | ||||
| chr4:37826590-37826732 | Common:1; Rare:55 | ||||
| chr4:39182227-39182548 | Rare:71; Clinvar:2 | ||||
| chr4:39366289-39366394 | Common:1; Rare:31 | ||||
| chr4:39458868-39459112 | Common:3; Rare:136; Clinvar (benign):5 | ||||
| chr4:39527383-39527755 | Common:2; Rare:91 | ||||
| chr4:39638834-39639149 | Common:1; Rare:115 | ||||
| chr4:39697981-39698185 | Common:1; Rare:82 |