| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:55949420-55949690 | Rare:44 | ||||
| chr4:56048821-56049173 | Common:3; Rare:97 | ||||
| chr4:56387084-56387263 | Rare:37 | ||||
| chr4:56387322-56387582 | Rare:88 | ||||
| chr4:56435475-56435782 | Common:5; Rare:107 | ||||
| chr4:56435955-56436313 | Rare:132 | ||||
| chr4:56467524-56467723 | Common:2; Rare:81; Clinvar (benign):5 | ||||
| chr4:56467750-56467900 | Common:1; Rare:53 | ||||
| chr4:56467938-56468254 | Common:2; Rare:64 | ||||
| chr4:56530376-56530673 | Common:5; Rare:74 | ||||
| chr4:56530710-56530990 | Common:3; Rare:76 | ||||
| chr4:56907753-56907942 | Common:2; Rare:82 | ||||
| chr4:56977547-56977792 | Common:2; Rare:92 | ||||
| chr4:56978729-56978907 | Common:4; Rare:43 | ||||
| chr4:57110720-57111110 | Common:2; Rare:70 |