| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132687332-132687587 | Common:1; Rare:92; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:132829062-132829216 | Rare:76 | ||||
| chr12:132887555-132887880 | Rare:96 | ||||
| chr12:132956252-132956370 | Common:1; Rare:29 | ||||
| chr12:133130385-133130652 | Common:6; Rare:96 | ||||
| chr13:19633886-19633959 | Rare:27 | ||||
| chr13:19863484-19863873 | Common:5; Rare:142 | ||||
| chr13:19958440-19958868 | Common:7; Rare:191 | ||||
| chr13:20525801-20526083 | Common:5; Rare:94 | ||||
| chr13:21140331-21140615 | Rare:130 | ||||
| chr13:21176531-21176696 | Common:1; Rare:77 | ||||
| chr13:25287303-25287622 | Common:2; Rare:96 | ||||
| chr13:25301401-25301684 | Common:1; Rare:100 | ||||
| chr13:26222300-26222522 | Common:4; Rare:58 | ||||
| chr13:27251282-27251684 | Common:4; Rare:111 |