| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:69359668-69359777 | Common:3; Rare:46 | ||||
| chr12:69470304-69470429 | Common:2; Rare:42 | ||||
| chr12:69585308-69585524 | Common:3; Rare:87 | ||||
| chr12:69610671-69611047 | Rare:95; Clinvar:5; Clinvar (benign):2 | ||||
| chr12:69738593-69738993 | Common:3; Rare:142 | ||||
| chr12:70610321-70610491 | Rare:35 | ||||
| chr12:70637388-70637550 | Rare:37 | ||||
| chr12:71663770-71664042 | Common:1; Rare:80 | ||||
| chr12:71664074-71664484 | Rare:109 | ||||
| chr12:71686035-71686129 | Common:1; Rare:29 | ||||
| chr12:71686205-71686420 | Common:1; Rare:64 | ||||
| chr12:71686425-71686539 | Common:1; Rare:31 | ||||
| chr12:71754737-71754873 | Common:2; Rare:32 | ||||
| chr12:71839593-71839821 | Common:1; Rare:89 | ||||
| chr12:74537753-74538011 | Common:1; Rare:87 |