| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:52051321-52051527 | Common:1; Rare:48 | ||||
| chr4:52659204-52659442 | Common:1; Rare:81 | ||||
| chr4:52862142-52862322 | Common:7; Rare:82 | ||||
| chr4:54228937-54229409 | Common:1; Rare:94; Clinvar (benign):4 | ||||
| chr4:54277154-54277441 | Common:2; Rare:60; Clinvar:5; Clinvar (benign):3 | ||||
| chr4:54657785-54658019 | Common:2; Rare:88; Clinvar (benign):1 | ||||
| chr4:55346126-55346324 | Common:3; Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:55395812-55395957 | Common:2; Rare:39; Clinvar:2 | ||||
| chr4:55398666-55398876 | Common:2; Rare:25 | ||||
| chr4:55546801-55546936 | Common:1; Rare:43 | ||||
| chr4:55948770-55948961 | Common:1; Rare:34 | ||||
| chr4:56387180-56387235 | Rare:12 | ||||
| chr4:56387419-56387543 | Rare:41 | ||||
| chr4:56435481-56435753 | Common:5; Rare:101 | ||||
| chr4:56467527-56467708 | Common:2; Rare:74; Clinvar (benign):5 |