| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6963049-6963240 | Common:1; Rare:36 | ||||
| chr12:7970715-7970789 | Rare:29 | ||||
| chr12:9283896-9284034 | Common:4; Rare:8 | ||||
| chr12:9647978-9648178 | Common:4; Rare:66 | ||||
| chr12:24562510-24562810 | Common:1; Rare:76 | ||||
| chr12:31119063-31119399 | Common:30; Rare:60 | ||||
| chr12:48863278-48863479 | Common:1; Rare:41 | ||||
| chr12:49060789-49060902 | Common:1; Rare:45 | ||||
| chr12:49234587-49234673 | Rare:22 | ||||
| chr12:53027851-53028182 | Common:1; Rare:113 | ||||
| chr12:54081880-54081978 | Common:1; Rare:16 | ||||
| chr12:77324841-77325069 | Common:2; Rare:81 | ||||
| chr12:91381456-91381625 | Common:2; Rare:32 | ||||
| chr12:101761250-101761459 | Rare:50; Clinvar (pathogenic):2 | ||||
| chr12:103946663-103946920 | Rare:68 |