| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51968000-51968223 | Rare:60 | ||||
| chr3:51973679-51974550 | Rare:409 | ||||
| chr3:51975021-51975215 | Common:3; Rare:176 | ||||
| chr3:51982730-51983130 | Common:2; Rare:120 | ||||
| chr3:51983084-51983567 | Common:5; Rare:257 | ||||
| chr3:51995705-51996108 | Common:10; Rare:295 | ||||
| chr3:52056452-52056711 | Common:1; Rare:117 | ||||
| chr3:52154301-52154547 | Common:4; Rare:122; Clinvar (benign):1 | ||||
| chr3:52154632-52155046 | Common:12; Rare:190 | ||||
| chr3:52197935-52198222 | Common:2; Rare:256 | ||||
| chr3:52239038-52239305 | Common:6; Rare:230 | ||||
| chr3:52245653-52245770 | Rare:37 | ||||
| chr3:52245790-52246370 | Common:6; Rare:285 | ||||
| chr3:52277716-52277855 | Common:1; Rare:42 | ||||
| chr3:52277757-52278378 | Common:3; Rare:275 |