| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120224700-120224823 | Common:2; Rare:40 | ||||
| chr12:120437828-120438228 | Common:4; Rare:283; Clinvar (benign):4 | ||||
| chr12:120446343-120446495 | Common:3; Rare:133 | ||||
| chr12:120469511-120469878 | Common:6; Rare:239 | ||||
| chr12:120495825-120496204 | Common:14; Rare:226 | ||||
| chr12:120528936-120529251 | Common:4; Rare:220 | ||||
| chr12:120534258-120534414 | Common:2; Rare:96 | ||||
| chr12:120534780-120535390 | Common:2; Rare:360 | ||||
| chr12:120581309-120581586 | Common:2; Rare:198 | ||||
| chr12:120686930-120687196 | Common:4; Rare:179 | ||||
| chr12:120687200-120687536 | Common:1; Rare:119 | ||||
| chr12:120902910-120903720 | Common:17; Rare:215 | ||||
| chr12:120904274-120904478 | Common:5; Rare:152 | ||||
| chr12:121038901-121039397 | Common:6; Rare:164 | ||||
| chr12:121296655-121296897 | Common:2; Rare:135 |