| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73071650-73071920 | Common:3; Rare:110 | ||||
| chr2:73072144-73072309 | Rare:44 | ||||
| chr2:73214124-73214335 | Common:1; Rare:78 | ||||
| chr2:73214429-73214764 | Common:3; Rare:115 | ||||
| chr2:73233130-73233578 | Common:3; Rare:139 | ||||
| chr2:73233674-73233775 | Rare:16 | ||||
| chr2:73234171-73234421 | Common:2; Rare:83 | ||||
| chr2:73234549-73234760 | Rare:70 | ||||
| chr2:73269484-73269614 | Rare:20 | ||||
| chr2:73284228-73284701 | Common:1; Rare:120 | ||||
| chr2:73284742-73284973 | Common:1; Rare:51 | ||||
| chr2:73293546-73293818 | Common:1; Rare:111 | ||||
| chr2:73385520-73385788 | Rare:82; Clinvar:1 | ||||
| chr2:73385968-73386410 | Common:1; Rare:187; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr2:73737203-73737659 | Common:3; Rare:148 |