| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125625871-125625974 | Rare:35 | ||||
| chr11:126211634-126211804 | Rare:77 | ||||
| chr11:126268829-126269171 | Common:1; Rare:124; Clinvar:1 | ||||
| chr11:126303961-126304073 | Rare:62 | ||||
| chr11:131911386-131911492 | Common:1; Rare:47 | ||||
| chr11:134253306-134253586 | Common:2; Rare:90; Clinvar (benign):1 | ||||
| chr12:2877027-2877262 | Rare:70 | ||||
| chr12:4320949-4321258 | Common:5; Rare:117 | ||||
| chr12:4538452-4538896 | Common:1; Rare:94 | ||||
| chr12:4648994-4649130 | Common:1; Rare:38 | ||||
| chr12:6493241-6493502 | Common:6; Rare:78 | ||||
| chr12:6493788-6494119 | Common:2; Rare:100 | ||||
| chr12:6568260-6568371 | Rare:42 | ||||
| chr12:6723855-6724132 | Common:1; Rare:52 | ||||
| chr12:6867387-6867540 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):2 |