| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42631039-42631171 | Rare:24 | ||||
| chr3:42773220-42773348 | Common:1; Rare:34 | ||||
| chr3:42804265-42804663 | Common:2; Rare:107 | ||||
| chr3:43286400-43286641 | Common:2; Rare:106 | ||||
| chr3:43621890-43622316 | Common:2; Rare:123; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690458-43691023 | Common:8; Rare:212; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:43691554-43691683 | Common:1; Rare:23 | ||||
| chr3:44338057-44338187 | Common:2; Rare:45 | ||||
| chr3:44338241-44338524 | Common:3; Rare:92 | ||||
| chr3:44338702-44338815 | Common:3; Rare:42 | ||||
| chr3:44477618-44477803 | Common:1; Rare:42 | ||||
| chr3:44584715-44585023 | Rare:57 | ||||
| chr3:44624922-44625103 | Common:2; Rare:51 | ||||
| chr3:44648639-44648811 | Rare:42 | ||||
| chr3:44712577-44712720 | Common:1; Rare:58 |