| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12717219-12717562 | Common:1; Rare:111; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12717585-12717746 | Rare:41; Clinvar (benign):2 | ||||
| chr12:12717754-12717954 | Common:1; Rare:73; Clinvar:11; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr12:12725242-12725545 | Common:3; Rare:73 | ||||
| chr12:12725642-12725983 | Common:3; Rare:78 | ||||
| chr12:12952153-12952466 | Common:3; Rare:54 | ||||
| chr12:12989276-12989594 | Rare:86 | ||||
| chr12:13000176-13000486 | Common:2; Rare:96 | ||||
| chr12:14365448-14365763 | Common:1; Rare:101 | ||||
| chr12:14365959-14366066 | Rare:29 | ||||
| chr12:14567638-14567976 | Common:3; Rare:75 | ||||
| chr12:14774184-14774501 | Common:3; Rare:84 | ||||
| chr12:14803435-14803715 | Common:1; Rare:74 | ||||
| chr12:14843343-14843694 | Common:1; Rare:70 | ||||
| chr12:14884217-14884539 | Common:3; Rare:62; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 |