| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:168481414-168481505 | Rare:13 | ||||
| chr4:168604671-168604845 | Common:2; Rare:35 | ||||
| chr4:168608244-168608525 | Common:3; Rare:51 | ||||
| chr4:168630913-168630970 | Rare:8 | ||||
| chr4:168643255-168643275 | Rare:3 | ||||
| chr4:168648169-168648259 | Rare:14 | ||||
| chr4:168797262-168797372 | Common:3; Rare:13 | ||||
| chr4:168832984-168833121 | Common:3; Rare:37 | ||||
| chr4:168849076-168849246 | Common:1; Rare:41 | ||||
| chr4:168877793-168877946 | Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:168878253-168878272 | Rare:5; Clinvar (benign):1 | ||||
| chr4:168960846-168960998 | Rare:35 | ||||
| chr4:169018018-169018187 | Common:2; Rare:27 | ||||
| chr4:169070422-169070495 | Common:1; Rare:12 | ||||
| chr4:169079961-169080075 | Common:2; Rare:21 |