| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120534912-120535021 | Rare:47 | ||||
| chr12:120535040-120535136 | Rare:18 | ||||
| chr12:120535207-120535261 | Rare:13 | ||||
| chr12:120581175-120581215 | Rare:12 | ||||
| chr12:120581313-120581612 | Common:2; Rare:115 | ||||
| chr12:120640458-120640658 | Rare:53 | ||||
| chr12:120686326-120686874 | Common:3; Rare:140 | ||||
| chr12:120686910-120687190 | Common:2; Rare:98 | ||||
| chr12:120710282-120710560 | Common:3; Rare:99 | ||||
| chr12:120725670-120725908 | Common:3; Rare:74; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:120903411-120903662 | Rare:52 | ||||
| chr12:120903663-120903852 | Common:3; Rare:61 | ||||
| chr12:120904078-120904182 | Common:1; Rare:28 | ||||
| chr12:120904230-120904527 | Common:3; Rare:113 | ||||
| chr12:121016182-121016231 | Rare:14 |