| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:55546467-55547041 | Common:15; Rare:361 | ||||
| chr4:55547410-55547640 | Common:2; Rare:70 | ||||
| chr4:55636218-55636464 | Common:2; Rare:65 | ||||
| chr4:55853448-55853860 | Rare:314 | ||||
| chr4:55854001-55854109 | Rare:16 | ||||
| chr4:55948690-55949020 | Common:5; Rare:189 | ||||
| chr4:55949060-55949325 | Common:2; Rare:129 | ||||
| chr4:55949350-55949630 | Rare:46 | ||||
| chr4:56048937-56049261 | Common:3; Rare:136 | ||||
| chr4:56386971-56387371 | Rare:182 | ||||
| chr4:56387333-56387591 | Rare:216 | ||||
| chr4:56435414-56435831 | Common:15; Rare:366 | ||||
| chr4:56435951-56436538 | Rare:422 | ||||
| chr4:56467282-56467813 | Common:8; Rare:406; Clinvar (benign):15 | ||||
| chr4:56468036-56468247 | Rare:41 |