| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:72148465-72148649 | Rare:45 | ||||
| chr2:72887225-72887433 | Common:2; Rare:125; Clinvar (benign):2 | ||||
| chr2:73071225-73071355 | Common:1; Rare:44 | ||||
| chr2:73071698-73071861 | Common:4; Rare:122 | ||||
| chr2:73112854-73113013 | Common:3; Rare:39 | ||||
| chr2:73214172-73214343 | Common:2; Rare:108 | ||||
| chr2:73214473-73214647 | Common:2; Rare:60 | ||||
| chr2:73233200-73233508 | Common:2; Rare:165 | ||||
| chr2:73234193-73234364 | Common:3; Rare:92 | ||||
| chr2:73284263-73284580 | Common:2; Rare:154 | ||||
| chr2:73284720-73285020 | Common:1; Rare:81 | ||||
| chr2:73385500-73386138 | Common:6; Rare:340; Clinvar:24; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr2:73386202-73386345 | Common:1; Rare:52; Clinvar (benign):2 | ||||
| chr2:73737276-73737541 | Common:6; Rare:168 | ||||
| chr2:73828801-73829054 | Common:3; Rare:112 |