| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:2963324-2963629 | Common:3; Rare:113 | ||||
| chr4:3292740-3293052 | Common:2; Rare:121 | ||||
| chr4:4248109-4248262 | Common:5; Rare:82 | ||||
| chr4:4290114-4290218 | Common:1; Rare:44 | ||||
| chr4:4541972-4542158 | Common:1; Rare:78 | ||||
| chr4:6640543-6640726 | Common:3; Rare:76 | ||||
| chr4:6986999-6987292 | Common:2; Rare:95 | ||||
| chr4:8592603-8592876 | Common:9; Rare:119 | ||||
| chr4:15681559-15681761 | Common:3; Rare:65 | ||||
| chr4:17810681-17811012 | Common:2; Rare:103 | ||||
| chr4:25160405-25160736 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233853-25234061 | Rare:90 | ||||
| chr4:25914051-25914288 | Common:2; Rare:101 | ||||
| chr4:26430516-26430768 | Rare:58 | ||||
| chr4:37826635-37826729 | Common:1; Rare:37 |