| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:55319038-55319505 | Common:3; Rare:136 | ||||
| chr15:55407996-55408317 | Common:4; Rare:88 | ||||
| chr15:55498221-55498267 | Rare:22; Clinvar (benign):1 | ||||
| chr15:55498277-55498540 | Common:5; Rare:107; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:55587838-55588016 | Common:1; Rare:60 | ||||
| chr15:55588108-55588266 | Common:2; Rare:56 | ||||
| chr15:55588314-55588444 | Rare:37 | ||||
| chr15:55588828-55589117 | Common:4; Rare:63 | ||||
| chr15:55742412-55742691 | Common:1; Rare:95 | ||||
| chr15:55742967-55743385 | Common:7; Rare:169 | ||||
| chr15:55743473-55743538 | Common:2; Rare:15 | ||||
| chr15:55993097-55993155 | Rare:16 | ||||
| chr15:55993309-55993428 | Common:2; Rare:35 | ||||
| chr15:55993557-55993766 | Common:1; Rare:70 | ||||
| chr15:56243433-56243470 | Rare:8 |