| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52705537-52705628 | Common:1; Rare:16 | ||||
| chr3:52705649-52706227 | Common:3; Rare:192 | ||||
| chr3:52770541-52770703 | Rare:42 | ||||
| chr3:52770785-52771172 | Common:6; Rare:109 | ||||
| chr3:52779677-52779831 | Common:1; Rare:26 | ||||
| chr3:52897506-52897757 | Rare:91 | ||||
| chr3:53045229-53045715 | Common:3; Rare:131 | ||||
| chr3:53046057-53046192 | Common:3; Rare:37 | ||||
| chr3:53046572-53046718 | Common:1; Rare:32 | ||||
| chr3:53130291-53130708 | Common:1; Rare:136; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:53160695-53160839 | Rare:33 | ||||
| chr3:53161032-53161317 | Common:5; Rare:71 | ||||
| chr3:53161428-53161632 | Rare:46 | ||||
| chr3:53255600-53255756 | Common:1; Rare:45 | ||||
| chr3:53255948-53256249 | Common:5; Rare:118 |