| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169270866-169271063 | Common:1; Rare:63 | ||||
| chr4:169612478-169612771 | Common:6; Rare:101; Clinvar:5; Clinvar (benign):2 | ||||
| chr4:169620381-169620652 | Common:2; Rare:103 | ||||
| chr4:169660036-169660261 | Common:1; Rare:42 | ||||
| chr4:169757829-169758069 | Common:2; Rare:78 | ||||
| chr4:170026293-170026599 | Common:4; Rare:117 | ||||
| chr4:173168200-173168365 | Common:1; Rare:38 | ||||
| chr4:173168576-173168940 | Common:3; Rare:116 | ||||
| chr4:173334272-173334761 | Rare:123 | ||||
| chr4:173335144-173335308 | Common:1; Rare:36 | ||||
| chr4:173369780-173369938 | Common:1; Rare:53 | ||||
| chr4:173370651-173371015 | Common:2; Rare:93 | ||||
| chr4:173371154-173371466 | Common:3; Rare:107 | ||||
| chr4:174283627-174284060 | Common:1; Rare:94 | ||||
| chr4:176319720-176320074 | Common:5; Rare:119 |