| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48634795-48635060 | Common:2; Rare:105 | ||||
| chr3:48635191-48635690 | Common:5; Rare:294 | ||||
| chr3:48662720-48663120 | Rare:206 | ||||
| chr3:48685390-48685760 | Rare:107 | ||||
| chr3:48685798-48686002 | Common:2; Rare:122 | ||||
| chr3:48717001-48717706 | Common:8; Rare:212 | ||||
| chr3:48846990-48847417 | Rare:206 | ||||
| chr3:48847586-48848016 | Common:3; Rare:277 | ||||
| chr3:48898814-48899091 | Rare:141; Clinvar:12 | ||||
| chr3:48918643-48918980 | Common:6; Rare:378 | ||||
| chr3:48919004-48919460 | Common:2; Rare:209 | ||||
| chr3:48989691-48990050 | Rare:195 | ||||
| chr3:48990137-48990560 | Rare:276 | ||||
| chr3:48990710-48991190 | Rare:184 | ||||
| chr3:49007102-49007569 | Common:6; Rare:414 |