| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37826588-37826729 | Common:1; Rare:54 | ||||
| chr4:39182267-39182548 | Rare:64; Clinvar:2 | ||||
| chr4:39366321-39366426 | Rare:33 | ||||
| chr4:39458843-39459065 | Common:3; Rare:121 | ||||
| chr4:39527359-39527733 | Common:2; Rare:86 | ||||
| chr4:39638850-39639158 | Common:1; Rare:114 | ||||
| chr4:44726484-44726631 | Common:2; Rare:53 | ||||
| chr4:48016643-48016784 | Common:1; Rare:42 | ||||
| chr4:52659231-52659539 | Common:1; Rare:95 | ||||
| chr4:56435484-56435927 | Common:6; Rare:140 | ||||
| chr4:56436029-56436320 | Rare:106 | ||||
| chr4:56467542-56467679 | Common:2; Rare:61; Clinvar (benign):4 | ||||
| chr4:56977513-56977745 | Common:2; Rare:86 | ||||
| chr4:57110069-57110182 | Rare:42 | ||||
| chr4:67701097-67701419 | Common:4; Rare:149 |