| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:119877632-119877752 | Rare:23 | ||||
| chr12:119990505-119990703 | Common:3; Rare:49 | ||||
| chr12:120116685-120117065 | Common:7; Rare:131 | ||||
| chr12:120117085-120117222 | Rare:33 | ||||
| chr12:120117456-120117557 | Rare:21 | ||||
| chr12:120117573-120117612 | Rare:9 | ||||
| chr12:120194687-120195132 | Common:3; Rare:119 | ||||
| chr12:120201043-120201396 | Common:2; Rare:117 | ||||
| chr12:120224684-120225039 | Common:3; Rare:93 | ||||
| chr12:120225958-120226120 | Common:1; Rare:25 | ||||
| chr12:120265674-120265968 | Common:1; Rare:109 | ||||
| chr12:120437775-120438210 | Common:2; Rare:150; Clinvar (benign):2 | ||||
| chr12:120446277-120446599 | Common:3; Rare:127 | ||||
| chr12:120446743-120446911 | Common:1; Rare:51; Clinvar (pathogenic):1 | ||||
| chr12:120469666-120469942 | Common:2; Rare:99 |