| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:6987006-6987303 | Common:2; Rare:94 | ||||
| chr4:7068030-7068373 | Common:5; Rare:117 | ||||
| chr4:8436020-8436139 | Common:1; Rare:21 | ||||
| chr4:8440717-8440813 | Rare:40 | ||||
| chr4:15427942-15428057 | Rare:12 | ||||
| chr4:15655289-15655477 | Common:1; Rare:84 | ||||
| chr4:15681564-15681869 | Common:3; Rare:107 | ||||
| chr4:17614551-17614651 | Common:2; Rare:43 | ||||
| chr4:17810687-17811065 | Common:4; Rare:119 | ||||
| chr4:23890004-23890134 | Rare:20 | ||||
| chr4:23904073-23904346 | Rare:49 | ||||
| chr4:25160411-25160727 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914051-25914328 | Common:2; Rare:118 | ||||
| chr4:26320743-26321041 | Rare:124; Clinvar (benign):1 | ||||
| chr4:37826419-37826729 | Common:8; Rare:102 |