| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:914429-914719 | Rare:79 | ||||
| chr12:991101-991330 | Common:3; Rare:102 | ||||
| chr12:2004427-2004626 | Common:1; Rare:70 | ||||
| chr12:2794989-2795238 | Rare:99 | ||||
| chr12:2796836-2797276 | Common:1; Rare:95 | ||||
| chr12:2801048-2801167 | Common:1; Rare:40 | ||||
| chr12:2812619-2812714 | Rare:31 | ||||
| chr12:2812880-2813076 | Rare:55 | ||||
| chr12:2877017-2877277 | Rare:86 | ||||
| chr12:2959843-2959973 | Common:1; Rare:32 | ||||
| chr12:3077289-3077428 | Common:4; Rare:61 | ||||
| chr12:4320949-4321260 | Common:5; Rare:118 | ||||
| chr12:4538436-4538786 | Rare:74 | ||||
| chr12:4649010-4649154 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr12:6200042-6200559 | Common:4; Rare:152 |