| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:111842584-111842984 | Common:2; Rare:182 | ||||
| chr12:112005949-112006560 | Common:10; Rare:254 | ||||
| chr12:112012460-112013009 | Common:4; Rare:227 | ||||
| chr12:112013027-112013548 | Common:7; Rare:1061 | ||||
| chr12:112013650-112014392 | Common:1; Rare:276 | ||||
| chr12:112019051-112019832 | Rare:226 | ||||
| chr12:112108552-112109233 | Common:4; Rare:396 | ||||
| chr12:112109234-112109760 | Common:2; Rare:129 | ||||
| chr12:112125226-112125639 | Rare:239 | ||||
| chr12:112381578-112382603 | Common:7; Rare:802 | ||||
| chr12:112408262-112409112 | Common:4; Rare:345 | ||||
| chr12:112409132-112409855 | Common:6; Rare:512 | ||||
| chr12:112417820-112418642 | Common:2; Rare:240 | ||||
| chr12:112418670-112419394 | Common:8; Rare:440; Clinvar:13; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr12:112938155-112938640 | Common:12; Rare:282 |