| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109111029-109111237 | Common:1; Rare:58 | ||||
| chr12:114399606-114399891 | Rare:73; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:114401013-114401096 | Rare:26 | ||||
| chr12:120291901-120292189 | Common:8; Rare:113 | ||||
| chr12:122382962-122383271 | Rare:66 | ||||
| chr12:124939862-124939960 | Common:2; Rare:43 | ||||
| chr13:20772985-20773288 | Common:2; Rare:50 | ||||
| chr13:21298026-21298186 | Common:3; Rare:41 | ||||
| chr13:29140318-29140578 | Rare:42 | ||||
| chr13:33106783-33107150 | Common:2; Rare:81 | ||||
| chr13:35475408-35475652 | Rare:80 | ||||
| chr13:42271385-42271533 | Common:1; Rare:48 | ||||
| chr13:52194378-52194494 | Rare:36 | ||||
| chr13:57629927-57630126 | Common:1; Rare:53 | ||||
| chr13:76884456-76884592 | Rare:25 |