| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48105815-48105941 | Rare:30 | ||||
| chr12:48105979-48106086 | Rare:29 | ||||
| chr12:48106091-48106149 | Common:2; Rare:20 | ||||
| chr12:48682196-48682467 | Common:6; Rare:83 | ||||
| chr12:48716687-48716989 | Common:4; Rare:95 | ||||
| chr12:49018741-49018928 | Common:1; Rare:74 | ||||
| chr12:49131304-49131603 | Common:2; Rare:121 | ||||
| chr12:49188998-49189281 | Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264781-49265096 | Common:4; Rare:114 | ||||
| chr12:49322964-49323323 | Common:3; Rare:87 | ||||
| chr12:49367159-49367554 | Common:1; Rare:109 | ||||
| chr12:49568104-49568190 | Common:2; Rare:28 | ||||
| chr12:49843092-49843192 | Common:1; Rare:35 | ||||
| chr12:50085046-50085355 | Rare:83 | ||||
| chr12:50283515-50283654 | Common:1; Rare:42 |