| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104064027-104064199 | Rare:36 | ||||
| chr12:104064430-104064628 | Rare:53 | ||||
| chr12:104138142-104138371 | Rare:54 | ||||
| chr12:104958211-104958461 | Common:4; Rare:75 | ||||
| chr12:104986201-104986375 | Common:4; Rare:64 | ||||
| chr12:105107605-105107789 | Common:1; Rare:82 | ||||
| chr12:105236049-105236312 | Common:2; Rare:116 | ||||
| chr12:106357426-106357823 | Common:4; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106357952-106358126 | Common:3; Rare:80 | ||||
| chr12:106774533-106774714 | Common:1; Rare:55 | ||||
| chr12:106774898-106775183 | Rare:72 | ||||
| chr12:106955460-106955869 | Common:3; Rare:146 | ||||
| chr12:107685709-107685934 | Rare:74 | ||||
| chr12:108515021-108515289 | Common:1; Rare:80 | ||||
| chr12:108561136-108561461 | Common:4; Rare:80 |