| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52705500-52706188 | Common:5; Rare:211 | ||||
| chr3:52770916-52770999 | Common:2; Rare:22 | ||||
| chr3:53255837-53256079 | Common:1; Rare:81 | ||||
| chr3:53846392-53846571 | Rare:57 | ||||
| chr3:53891807-53892075 | Common:4; Rare:90 | ||||
| chr3:56557086-56557238 | Common:2; Rare:60 | ||||
| chr3:57079257-57079382 | Common:2; Rare:42 | ||||
| chr3:57227588-57227925 | Common:4; Rare:113 | ||||
| chr3:57556000-57556321 | Rare:80 | ||||
| chr3:57597277-57597732 | Common:4; Rare:140 | ||||
| chr3:57692794-57692828 | Rare:11 | ||||
| chr3:57692966-57693170 | Common:1; Rare:60 | ||||
| chr3:58008323-58008661 | Common:1; Rare:114; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:58165289-58165494 | Rare:33 | ||||
| chr3:58306485-58306590 | Common:3; Rare:43 |