| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51941968-51942427 | Common:2; Rare:117 | ||||
| chr3:51942944-51943300 | Common:1; Rare:52 | ||||
| chr3:51975052-51975142 | Common:1; Rare:33 | ||||
| chr3:51983303-51983547 | Rare:58 | ||||
| chr3:52239079-52239255 | Common:2; Rare:64 | ||||
| chr3:52278625-52278774 | Rare:53 | ||||
| chr3:52287737-52287859 | Common:2; Rare:49 | ||||
| chr3:52455414-52455648 | Common:2; Rare:76 | ||||
| chr3:52479992-52480163 | Common:2; Rare:31 | ||||
| chr3:52495282-52495410 | Common:1; Rare:36 | ||||
| chr3:52525051-52525216 | Common:8; Rare:78 | ||||
| chr3:52685544-52686100 | Common:4; Rare:183 | ||||
| chr3:52705576-52706269 | Common:4; Rare:228 | ||||
| chr3:52770894-52771038 | Common:3; Rare:40 | ||||
| chr3:53130387-53130509 | Rare:48; Clinvar:1; Clinvar (benign):3 |