| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40309486-40309809 | Common:9; Rare:111 | ||||
| chr3:42581879-42582199 | Common:3; Rare:95 | ||||
| chr3:42582272-42582343 | Rare:19 | ||||
| chr3:42804435-42804663 | Common:2; Rare:69 | ||||
| chr3:44624852-44625080 | Common:2; Rare:67 | ||||
| chr3:44761603-44761794 | Common:3; Rare:66 | ||||
| chr3:44976142-44976287 | Common:2; Rare:59 | ||||
| chr3:47475815-47476069 | Common:3; Rare:106 | ||||
| chr3:48301365-48301490 | Common:1; Rare:27 | ||||
| chr3:48440039-48440270 | Common:1; Rare:70 | ||||
| chr3:48918764-48918900 | Common:2; Rare:80 | ||||
| chr3:49007030-49007426 | Common:2; Rare:137 | ||||
| chr3:49022011-49022145 | Rare:43; Clinvar:2 | ||||
| chr3:49121834-49121954 | Common:2; Rare:40; Clinvar (benign):1 | ||||
| chr3:49340000-49340108 | Common:2; Rare:55 |