| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50328177-50328362 | Rare:54 | ||||
| chr3:50350731-50350866 | Common:1; Rare:18 | ||||
| chr3:51385025-51385299 | Rare:77 | ||||
| chr3:51499961-51500065 | Rare:24 | ||||
| chr3:51975021-51975138 | Common:1; Rare:42 | ||||
| chr3:52239089-52239245 | Common:2; Rare:57 | ||||
| chr3:52287796-52287850 | Rare:24 | ||||
| chr3:52455425-52455634 | Common:2; Rare:66 | ||||
| chr3:52536354-52536699 | Common:2; Rare:110 | ||||
| chr3:52685836-52686041 | Common:1; Rare:73 | ||||
| chr3:52705771-52706219 | Common:2; Rare:156 | ||||
| chr3:52770913-52771052 | Common:2; Rare:32 | ||||
| chr3:53130396-53130568 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53255945-53256168 | Common:3; Rare:91 | ||||
| chr3:53347525-53347752 | Common:1; Rare:69 |