| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:14774918-14775034 | Rare:20 | ||||
| chr12:14802954-14803152 | Common:4; Rare:50 | ||||
| chr12:14803435-14803715 | Common:1; Rare:74 | ||||
| chr12:14843245-14843506 | Rare:44 | ||||
| chr12:14884211-14884545 | Common:3; Rare:63; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:14885721-14885980 | Common:3; Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:15221194-15221574 | Common:1; Rare:105 | ||||
| chr12:15882319-15882741 | Common:1; Rare:133 | ||||
| chr12:16347482-16347897 | Common:5; Rare:76 | ||||
| chr12:16608068-16608376 | Rare:73 | ||||
| chr12:19129402-19129808 | Common:3; Rare:167 | ||||
| chr12:19440379-19440636 | Common:2; Rare:96 | ||||
| chr12:21501525-21501866 | Common:4; Rare:93 | ||||
| chr12:21774570-21775040 | Rare:89 | ||||
| chr12:21941214-21941445 | Rare:57 |