| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123584297-123584808 | Common:9; Rare:172 | ||||
| chr12:123633562-123633840 | Common:1; Rare:134; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972568-123972646 | Common:3; Rare:25 | ||||
| chr12:123973070-123973281 | Common:2; Rare:65 | ||||
| chr12:132144310-132144489 | Rare:73 | ||||
| chr12:132956271-132956370 | Common:1; Rare:25 | ||||
| chr12:133130271-133130611 | Common:7; Rare:105 | ||||
| chr13:19863484-19863618 | Common:2; Rare:46 | ||||
| chr13:20525793-20526107 | Common:5; Rare:102 | ||||
| chr13:21176575-21176696 | Rare:62 | ||||
| chr13:24512737-24512847 | Common:3; Rare:34 | ||||
| chr13:27450175-27450246 | Common:2; Rare:20 | ||||
| chr13:28659045-28659184 | Rare:62; Clinvar (pathogenic):1 | ||||
| chr13:30307005-30307204 | Common:4; Rare:46 | ||||
| chr13:30617803-30617984 | Common:1; Rare:62 |