| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8066335-8066569 | Rare:32 | ||||
| chr12:8662761-8663070 | Common:2; Rare:67 | ||||
| chr12:8697740-8698043 | Common:1; Rare:121 | ||||
| chr12:9760893-9761010 | Rare:15 | ||||
| chr12:10212824-10212944 | Rare:30 | ||||
| chr12:10613534-10613686 | Common:1; Rare:62 | ||||
| chr12:11171567-11171711 | Common:2; Rare:48 | ||||
| chr12:12357004-12357104 | Common:1; Rare:49 | ||||
| chr12:13000204-13000460 | Common:1; Rare:84 | ||||
| chr12:14771119-14771143 | Rare:17 | ||||
| chr12:14774184-14774609 | Common:3; Rare:129 | ||||
| chr12:14803409-14803699 | Common:2; Rare:78 | ||||
| chr12:14885744-14885936 | Common:3; Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:14961554-14961863 | Common:2; Rare:76 | ||||
| chr12:15882290-15882431 | Rare:53 |