| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:27971721-27972018 | Common:5; Rare:49 | ||||
| chr12:27972334-27972941 | Common:7; Rare:110 | ||||
| chr12:28133300-28133332 | Rare:5 | ||||
| chr12:28190341-28190635 | Common:2; Rare:90 | ||||
| chr12:29149019-29149352 | Rare:95 | ||||
| chr12:30695732-30695989 | Common:4; Rare:69 | ||||
| chr12:30754790-30755088 | Common:1; Rare:121 | ||||
| chr12:31073791-31073902 | Common:1; Rare:46 | ||||
| chr12:31073920-31074295 | Common:4; Rare:86 | ||||
| chr12:31324070-31324262 | Rare:51 | ||||
| chr12:31728990-31729277 | Common:1; Rare:91 | ||||
| chr12:31959262-31959482 | Common:2; Rare:70 | ||||
| chr12:32399746-32399939 | Common:1; Rare:64 | ||||
| chr12:32400105-32400159 | Rare:15 | ||||
| chr12:32740064-32740516 | Common:2; Rare:122; Clinvar:2; Clinvar (benign):3 |