| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51239119-51239303 | Common:2; Rare:55 | ||||
| chr12:51270301-51270357 | Common:2; Rare:16 | ||||
| chr12:52055845-52056187 | Common:4; Rare:104 | ||||
| chr12:52191880-52192294 | Common:3; Rare:99 | ||||
| chr12:52192303-52192444 | Rare:37 | ||||
| chr12:52232912-52233632 | Common:5; Rare:208 | ||||
| chr12:52243982-52244319 | Common:4; Rare:62 | ||||
| chr12:52245777-52246528 | Common:3; Rare:128 | ||||
| chr12:52903683-52903996 | Common:7; Rare:64 | ||||
| chr12:52904967-52905257 | Common:4; Rare:81 | ||||
| chr12:52948829-52949570 | Common:3; Rare:204; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr12:52949582-52949731 | Common:2; Rare:49 | ||||
| chr12:52949739-52950071 | Rare:68 | ||||
| chr12:52950734-52951118 | Common:2; Rare:89 | ||||
| chr12:52951552-52951984 | Rare:101; Clinvar:4 |