| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130314395-130314497 | Common:1; Rare:31 | ||||
| chr11:130448518-130448652 | Rare:36 | ||||
| chr11:134068873-134069132 | Rare:126; Clinvar (pathogenic):1 | ||||
| chr11:134224541-134224670 | Rare:47 | ||||
| chr11:134253298-134253591 | Common:2; Rare:97; Clinvar (benign):1 | ||||
| chr12:389249-389347 | Rare:38 | ||||
| chr12:643616-643721 | Rare:19 | ||||
| chr12:991114-991339 | Common:4; Rare:97 | ||||
| chr12:2004430-2004669 | Common:2; Rare:73 | ||||
| chr12:2053470-2053605 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:2812638-2812713 | Rare:26 | ||||
| chr12:2877045-2877253 | Rare:62 | ||||
| chr12:2959853-2959973 | Common:1; Rare:30 | ||||
| chr12:4274122-4274232 | Rare:22 | ||||
| chr12:4275373-4275566 | Common:2; Rare:29 |