| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46616989-46617270 | Common:7; Rare:126 | ||||
| chr2:46699009-46699331 | Common:1; Rare:96 | ||||
| chr2:46915722-46915939 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916012-46916134 | Common:2; Rare:38 | ||||
| chr2:46941671-46941764 | Common:2; Rare:38; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:48440631-48440824 | Common:5; Rare:87 | ||||
| chr2:53786862-53787191 | Common:1; Rare:125 | ||||
| chr2:53970774-53971152 | Common:11; Rare:138 | ||||
| chr2:55050292-55050397 | Rare:44 | ||||
| chr2:55050441-55050871 | Common:7; Rare:133 | ||||
| chr2:55232249-55232398 | Common:2; Rare:34 | ||||
| chr2:55232586-55232872 | Common:2; Rare:117 | ||||
| chr2:55519423-55519757 | Common:1; Rare:93 | ||||
| chr2:58046614-58046893 | Common:2; Rare:85 | ||||
| chr2:58241316-58241383 | Rare:45; Clinvar:3; Clinvar (benign):1 |