| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104691418-104691652 | Common:3; Rare:40 | ||||
| chr12:104696513-104696647 | Rare:27 | ||||
| chr12:104725536-104725673 | Rare:29 | ||||
| chr12:104769012-104769047 | Rare:3 | ||||
| chr12:105109517-105109722 | Common:2; Rare:46 | ||||
| chr12:105109926-105110013 | Common:1; Rare:7 | ||||
| chr12:105115515-105115713 | Rare:52; Clinvar:2 | ||||
| chr12:105118288-105118531 | Rare:51; Clinvar:1 | ||||
| chr12:105119457-105119722 | Common:2; Rare:46 | ||||
| chr12:105120117-105120404 | Common:1; Rare:56 | ||||
| chr12:105125985-105126362 | Common:1; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:105142348-105142617 | Rare:58 | ||||
| chr12:105145694-105145873 | Common:1; Rare:24 | ||||
| chr12:105154113-105154325 | Common:1; Rare:43 | ||||
| chr12:105178375-105178413 | Rare:8 |