| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149657878-149658162 | Common:1; Rare:61 | ||||
| chr3:149658480-149658666 | Common:1; Rare:44 | ||||
| chr3:149812990-149813311 | Common:2; Rare:106 | ||||
| chr3:150408226-150408361 | Common:1; Rare:67 | ||||
| chr3:150408490-150408660 | Rare:56 | ||||
| chr3:150410527-150410787 | Common:2; Rare:99 | ||||
| chr3:150603139-150603409 | Common:2; Rare:109 | ||||
| chr3:152244191-152244392 | Common:1; Rare:28 | ||||
| chr3:152268393-152268459 | Rare:9 | ||||
| chr3:152268471-152269388 | Common:3; Rare:309; Clinvar (benign):1 | ||||
| chr3:152269501-152269772 | Common:2; Rare:79 | ||||
| chr3:152269836-152270094 | Common:4; Rare:64 | ||||
| chr3:154121241-154121463 | Common:3; Rare:96 | ||||
| chr3:154324306-154324522 | Rare:94 | ||||
| chr3:155854318-155854811 | Common:1; Rare:136; Clinvar (benign):1 |