| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48198284-48198361 | Common:1; Rare:21 | ||||
| chr12:48231232-48231366 | Rare:17 | ||||
| chr12:48346708-48346984 | Common:1; Rare:39 | ||||
| chr12:48643722-48643775 | Rare:9 | ||||
| chr12:48663840-48664056 | Common:4; Rare:51 | ||||
| chr12:48701012-48701202 | Common:1; Rare:48 | ||||
| chr12:48779900-48780212 | Rare:56 | ||||
| chr12:48785105-48785221 | Rare:14 | ||||
| chr12:48787204-48787564 | Rare:65 | ||||
| chr12:48928289-48928459 | Common:1; Rare:33 | ||||
| chr12:49009113-49009149 | Rare:11 | ||||
| chr12:49021750-49022066 | Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:49029162-49029448 | Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:49060489-49060642 | Rare:47 | ||||
| chr12:49061039-49061352 | Common:1; Rare:64 |