| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:170089713-170090182 | Common:3; Rare:133 | ||||
| chr4:171812535-171812767 | Common:2; Rare:40 | ||||
| chr4:171812911-171813063 | Common:1; Rare:35 | ||||
| chr4:171813270-171813455 | Common:1; Rare:62 | ||||
| chr4:173168090-173168316 | Common:3; Rare:46 | ||||
| chr4:173168587-173168851 | Common:2; Rare:86 | ||||
| chr4:173369751-173369935 | Common:1; Rare:63 | ||||
| chr4:173370785-173370976 | Common:1; Rare:54 | ||||
| chr4:174282990-174283300 | Common:1; Rare:49 | ||||
| chr4:174283450-174284046 | Common:2; Rare:118 | ||||
| chr4:174522416-174522560 | Rare:49; Clinvar (pathogenic):1 | ||||
| chr4:174829220-174829424 | Common:1; Rare:42 | ||||
| chr4:175812207-175812858 | Common:11; Rare:146 | ||||
| chr4:176065674-176066121 | Common:7; Rare:133 | ||||
| chr4:176195575-176195722 | Common:1; Rare:55 |