| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15681478-15681879 | Common:4; Rare:139 | ||||
| chr4:17614555-17614660 | Common:2; Rare:45 | ||||
| chr4:17810677-17810996 | Common:2; Rare:98 | ||||
| chr4:20254128-20254239 | Rare:24 | ||||
| chr4:24912860-24913116 | Common:1; Rare:86 | ||||
| chr4:25160367-25160726 | Common:3; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914051-25914318 | Common:2; Rare:114 | ||||
| chr4:26320633-26320705 | Common:1; Rare:19 | ||||
| chr4:26320748-26321046 | Rare:127; Clinvar (benign):1 | ||||
| chr4:26860619-26860812 | Common:2; Rare:63 | ||||
| chr4:30719966-30720432 | Common:3; Rare:102 | ||||
| chr4:30722006-30722227 | Common:1; Rare:66 | ||||
| chr4:30724007-30724360 | Common:2; Rare:94 | ||||
| chr4:37826630-37826735 | Common:1; Rare:41 | ||||
| chr4:37890563-37890844 | Rare:64 |