| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43595961-43596196 | Common:1; Rare:82 | ||||
| chr2:45568013-45568154 | Common:2; Rare:29 | ||||
| chr2:46544043-46544286 | Rare:66 | ||||
| chr2:46616974-46617286 | Common:7; Rare:133 | ||||
| chr2:46915744-46915898 | Common:1; Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46941665-46941803 | Common:3; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:47905490-47905807 | Common:3; Rare:149 | ||||
| chr2:48314183-48314367 | Common:1; Rare:59 | ||||
| chr2:53786851-53787086 | Rare:80 | ||||
| chr2:53970990-53971152 | Common:5; Rare:73 | ||||
| chr2:55050414-55050754 | Common:4; Rare:103 | ||||
| chr2:55232262-55232759 | Common:4; Rare:145 | ||||
| chr2:55519411-55519760 | Common:1; Rare:100 | ||||
| chr2:58046600-58046875 | Common:2; Rare:87 | ||||
| chr2:60553623-60553663 | Rare:5 |