| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17810677-17811020 | Common:3; Rare:106 | ||||
| chr4:18021707-18021850 | Common:1; Rare:71 | ||||
| chr4:25160399-25160725 | Common:3; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25234007 | Rare:64 | ||||
| chr4:25312620-25312858 | Common:2; Rare:86 | ||||
| chr4:25863737-25863948 | Common:1; Rare:30 | ||||
| chr4:25914051-25914292 | Common:2; Rare:103 | ||||
| chr4:26320789-26321025 | Rare:97; Clinvar (benign):1 | ||||
| chr4:26857443-26857790 | Common:4; Rare:96 | ||||
| chr4:26860545-26860819 | Common:3; Rare:91 | ||||
| chr4:37826550-37826729 | Common:4; Rare:66 | ||||
| chr4:38805711-38805741 | Rare:3 | ||||
| chr4:39182165-39182560 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39366324-39366416 | Rare:29 | ||||
| chr4:39458857-39459112 | Common:3; Rare:147; Clinvar (benign):5 |