| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51941847-51942257 | Common:2; Rare:115 | ||||
| chr3:51942264-51942421 | Common:2; Rare:49 | ||||
| chr3:51967308-51967677 | Common:1; Rare:88 | ||||
| chr3:51968010-51968186 | Rare:39 | ||||
| chr3:51968311-51968574 | Common:1; Rare:53 | ||||
| chr3:51973428-51973740 | Common:4; Rare:69 | ||||
| chr3:51975048-51975084 | Rare:11 | ||||
| chr3:51982943-51983302 | Common:1; Rare:78 | ||||
| chr3:51983398-51983551 | Rare:36 | ||||
| chr3:52239009-52239268 | Common:2; Rare:87 | ||||
| chr3:52278625-52278784 | Rare:55 | ||||
| chr3:52287727-52287866 | Common:2; Rare:52 | ||||
| chr3:52403266-52403462 | Rare:66; Clinvar:7; Clinvar (benign):11 | ||||
| chr3:52455429-52455717 | Common:2; Rare:96 | ||||
| chr3:52483653-52484088 | Common:1; Rare:98 |