| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38138554-38138710 | Common:2; Rare:60; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:39051942-39052042 | Common:1; Rare:36 | ||||
| chr3:39107553-39107725 | Common:3; Rare:54 | ||||
| chr3:39153505-39153745 | Common:3; Rare:75 | ||||
| chr3:39383577-39383676 | Rare:21; Clinvar:1 | ||||
| chr3:39406497-39406763 | Common:6; Rare:111 | ||||
| chr3:40309457-40309890 | Common:9; Rare:142 | ||||
| chr3:40310026-40310273 | Common:1; Rare:67 | ||||
| chr3:40457213-40457436 | Common:5; Rare:106 | ||||
| chr3:40505945-40506115 | Rare:38 | ||||
| chr3:40524815-40525004 | Common:1; Rare:54 | ||||
| chr3:41199177-41199573 | Common:1; Rare:161 | ||||
| chr3:42159911-42160212 | Common:1; Rare:57 | ||||
| chr3:42581898-42582137 | Common:3; Rare:75 | ||||
| chr3:42600418-42600777 | Common:2; Rare:131 |