| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:13420226-13420464 | Common:1; Rare:69 | ||||
| chr3:13480018-13480324 | Common:2; Rare:77 | ||||
| chr3:14124728-14125093 | Common:4; Rare:105; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178880 | Common:2; Rare:165; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402375-14402632 | Common:1; Rare:69 | ||||
| chr3:14651486-14651807 | Rare:93 | ||||
| chr3:14947258-14947551 | Common:3; Rare:130 | ||||
| chr3:15065237-15065399 | Common:2; Rare:56 | ||||
| chr3:15206043-15206269 | Rare:86 | ||||
| chr3:15427501-15427623 | Rare:42 | ||||
| chr3:15601530-15601775 | Common:4; Rare:100; Clinvar:1 | ||||
| chr3:16264872-16265233 | Common:2; Rare:118 | ||||
| chr3:17742596-17742833 | Common:3; Rare:83 | ||||
| chr3:19946974-19947412 | Common:5; Rare:164 | ||||
| chr3:20186176-20186365 | Common:1; Rare:53 |