| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47758813-47759091 | Common:2; Rare:54 | ||||
| chr12:47773114-47773313 | Rare:80 | ||||
| chr12:47813031-47813253 | Rare:55 | ||||
| chr12:47819864-47820123 | Common:2; Rare:62 | ||||
| chr12:47904974-47905151 | Common:1; Rare:55; Clinvar:1 | ||||
| chr12:47963241-47963649 | Common:3; Rare:87 | ||||
| chr12:48105828-48105965 | Rare:37 | ||||
| chr12:48105972-48106218 | Common:2; Rare:83 | ||||
| chr12:48106276-48106365 | Rare:25 | ||||
| chr12:48119186-48119398 | Common:2; Rare:43; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48141270-48141356 | Common:1; Rare:18; Clinvar (benign):1 | ||||
| chr12:48183994-48184132 | Common:4; Rare:41 | ||||
| chr12:48350750-48350963 | Rare:72 | ||||
| chr12:48351236-48351375 | Common:2; Rare:25 | ||||
| chr12:48716679-48716941 | Common:4; Rare:82 |