| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:4541970-4542153 | Common:1; Rare:78 | ||||
| chr4:5019423-5019597 | Common:1; Rare:52 | ||||
| chr4:15681537-15681854 | Common:3; Rare:115 | ||||
| chr4:17810687-17811035 | Common:3; Rare:107 | ||||
| chr4:25160442-25160704 | Common:3; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:26320874-26321024 | Rare:51; Clinvar (benign):1 | ||||
| chr4:37826514-37826727 | Common:6; Rare:78 | ||||
| chr4:38867493-38867822 | Common:2; Rare:101 | ||||
| chr4:39366324-39366416 | Rare:29 | ||||
| chr4:39458888-39459089 | Common:2; Rare:105; Clinvar (benign):3 | ||||
| chr4:39638847-39639140 | Common:1; Rare:109 | ||||
| chr4:39697987-39698144 | Common:1; Rare:63 | ||||
| chr4:48341225-48341478 | Common:1; Rare:105 | ||||
| chr4:56435551-56435752 | Common:3; Rare:70 | ||||
| chr4:56467565-56467645 | Rare:31 |