| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:26320905-26321024 | Rare:42; Clinvar (benign):1 | ||||
| chr4:26584000-26584120 | Rare:23 | ||||
| chr4:37826514-37826723 | Common:6; Rare:77 | ||||
| chr4:37977143-37977447 | Rare:79 | ||||
| chr4:39366324-39366449 | Rare:39 | ||||
| chr4:39458849-39459112 | Common:3; Rare:149; Clinvar (benign):5 | ||||
| chr4:39527383-39527775 | Common:2; Rare:103 | ||||
| chr4:39527946-39528037 | Rare:23 | ||||
| chr4:39638847-39639199 | Common:1; Rare:137 | ||||
| chr4:39697997-39698192 | Common:1; Rare:75 | ||||
| chr4:40056668-40056950 | Common:4; Rare:92 | ||||
| chr4:41256693-41256994 | Common:4; Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:41935086-41935187 | Common:1; Rare:25 | ||||
| chr4:41990353-41990585 | Common:1; Rare:79 | ||||
| chr4:44678352-44678706 | Common:1; Rare:130 |