| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8227368-8227691 | Common:2; Rare:76 | ||||
| chr12:8914376-8914735 | Common:6; Rare:106 | ||||
| chr12:8949951-8950099 | Common:1; Rare:43 | ||||
| chr12:9115762-9116283 | Common:3; Rare:116 | ||||
| chr12:9869352-9869494 | Common:1; Rare:23 | ||||
| chr12:10613534-10613686 | Common:1; Rare:62 | ||||
| chr12:10721791-10722273 | Common:1; Rare:125 | ||||
| chr12:10722864-10723022 | Common:3; Rare:54 | ||||
| chr12:11170962-11171261 | Common:4; Rare:86 | ||||
| chr12:11171534-11171638 | Common:1; Rare:32 | ||||
| chr12:12356986-12357188 | Common:4; Rare:106 | ||||
| chr12:12560892-12561192 | Common:4; Rare:64 | ||||
| chr12:12611627-12611998 | Common:2; Rare:110 | ||||
| chr12:12696182-12696286 | Rare:29 | ||||
| chr12:12717185-12717502 | Rare:108; Clinvar:2; Clinvar (benign):1 |