| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48957390-48957744 | Common:5; Rare:89 | ||||
| chr12:49017765-49018486 | Common:1; Rare:143 | ||||
| chr12:49018567-49018947 | Common:4; Rare:143 | ||||
| chr12:49069974-49070144 | Common:2; Rare:42 | ||||
| chr12:49110173-49110329 | Common:2; Rare:35 | ||||
| chr12:49110650-49111064 | Rare:93 | ||||
| chr12:49130234-49130993 | Common:9; Rare:366 | ||||
| chr12:49131348-49131704 | Common:2; Rare:132 | ||||
| chr12:49189049-49189377 | Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:49322909-49323327 | Common:3; Rare:107 | ||||
| chr12:49366114-49366514 | Common:4; Rare:97 | ||||
| chr12:49366729-49366967 | Common:1; Rare:71 | ||||
| chr12:49367123-49367542 | Common:2; Rare:119 | ||||
| chr12:49538799-49539075 | Rare:60 | ||||
| chr12:49567849-49568455 | Common:2; Rare:145 |