| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26033776-26034258 | Common:4; Rare:174 | ||||
| chr2:26034317-26034732 | Common:3; Rare:101 | ||||
| chr2:26244564-26244998 | Common:2; Rare:159; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345789-26346160 | Common:1; Rare:111 | ||||
| chr2:26764188-26764347 | Common:2; Rare:62 | ||||
| chr2:27032841-27033051 | Rare:80 | ||||
| chr2:27050668-27050775 | Common:4; Rare:50 | ||||
| chr2:27051546-27051706 | Rare:49 | ||||
| chr2:27071324-27071864 | Common:2; Rare:168 | ||||
| chr2:27078524-27078768 | Common:2; Rare:64 | ||||
| chr2:27086537-27086797 | Common:3; Rare:76; Clinvar (benign):1 | ||||
| chr2:27211730-27212096 | Common:3; Rare:124 | ||||
| chr2:27212210-27212437 | Common:2; Rare:120 | ||||
| chr2:27217115-27217561 | Common:1; Rare:155 | ||||
| chr2:27323043-27323171 | Common:1; Rare:37; Clinvar (benign):1 |