| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:226062452-226062870 | Common:1; Rare:146 | ||||
| chr1:226186611-226187106 | Common:5; Rare:139 | ||||
| chr1:226187165-226187230 | Rare:14 | ||||
| chr1:226223399-226223528 | Common:2; Rare:27 | ||||
| chr1:226308454-226308576 | Rare:31 | ||||
| chr1:226308864-226309222 | Common:2; Rare:104 | ||||
| chr1:226407596-226407742 | Common:3; Rare:40 | ||||
| chr1:226407939-226408421 | Common:6; Rare:142 | ||||
| chr1:226737418-226737474 | Common:1; Rare:22 | ||||
| chr1:226737784-226737947 | Rare:41 | ||||
| chr1:226738166-226738711 | Common:3; Rare:142 | ||||
| chr1:226739056-226739228 | Common:1; Rare:43 | ||||
| chr1:226739230-226739503 | Common:5; Rare:52 | ||||
| chr1:226870490-226870740 | Common:3; Rare:82; Clinvar (benign):2 | ||||
| chr1:226939403-226939815 | Common:1; Rare:98 |