| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47705978-47706116 | Rare:62 | ||||
| chr12:47758849-47759011 | Rare:36 | ||||
| chr12:48106019-48106196 | Common:2; Rare:62 | ||||
| chr12:48119211-48119398 | Common:2; Rare:38; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48350796-48350962 | Rare:61 | ||||
| chr12:48716679-48716941 | Common:4; Rare:82 | ||||
| chr12:49018744-49018851 | Rare:49 | ||||
| chr12:49110661-49110959 | Rare:61 | ||||
| chr12:49131355-49131621 | Common:2; Rare:96 | ||||
| chr12:49188455-49188590 | Common:1; Rare:19 | ||||
| chr12:49188981-49189215 | Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264780-49265085 | Common:4; Rare:109 | ||||
| chr12:49323017-49323302 | Common:2; Rare:66 | ||||
| chr12:49367183-49367539 | Common:1; Rare:102 | ||||
| chr12:49568104-49568225 | Common:2; Rare:38 |