| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:20621370-20621510 | Rare:45 | ||||
| chr12:20655039-20655096 | Rare:12 | ||||
| chr12:20687938-20688082 | Rare:18 | ||||
| chr12:21448297-21448300 | |||||
| chr12:21468344-21468641 | Common:2; Rare:71 | ||||
| chr12:21475459-21475713 | Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:21500821-21500973 | Common:1; Rare:28 | ||||
| chr12:21503615-21503913 | Common:1; Rare:53 | ||||
| chr12:21508477-21508682 | Common:1; Rare:38 | ||||
| chr12:22005682-22005837 | Common:1; Rare:27 | ||||
| chr12:22058445-22058665 | Rare:51 | ||||
| chr12:22460550-22460602 | Rare:13 | ||||
| chr12:22505017-22505155 | Rare:19 | ||||
| chr12:22522328-22522606 | Common:1; Rare:42 | ||||
| chr12:22541976-22542069 | Common:1; Rare:13 |