| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32399838-32399885 | Rare:18 | ||||
| chr12:32679050-32679358 | Common:2; Rare:122; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755208-32755366 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:32755455-32755510 | Rare:20 | ||||
| chr12:32755853-32756028 | Common:1; Rare:63 | ||||
| chr12:32896764-32896981 | Common:1; Rare:72; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:38905491-38905820 | Common:6; Rare:98 | ||||
| chr12:38905941-38906141 | Common:2; Rare:46 | ||||
| chr12:38906179-38906335 | Rare:33 | ||||
| chr12:38906687-38906847 | Common:1; Rare:38 | ||||
| chr12:39443080-39443466 | Common:2; Rare:114; Clinvar:8; Clinvar (benign):5 | ||||
| chr12:40692275-40692550 | Common:1; Rare:86 | ||||
| chr12:42238153-42238462 | Common:1; Rare:100 | ||||
| chr12:42325922-42326229 | Common:2; Rare:96 | ||||
| chr12:43758735-43759016 | Common:2; Rare:80; Clinvar:2 |