| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:54419449-54419662 | Rare:36 | ||||
| chr12:55699759-55699952 | Rare:54; Clinvar:1 | ||||
| chr12:55707476-55707669 | Common:1; Rare:72; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:55707678-55708086 | Common:2; Rare:92; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:55716010-55716178 | Common:1; Rare:81 | ||||
| chr12:55720210-55720443 | Common:4; Rare:30; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:55725876-55726243 | Rare:83 | ||||
| chr12:55728277-55728521 | Rare:76 | ||||
| chr12:55728953-55729094 | Rare:24 | ||||
| chr12:55729671-55729816 | Rare:35 | ||||
| chr12:55829498-55829829 | Rare:106 | ||||
| chr12:55830744-55830947 | Rare:64 | ||||
| chr12:55839636-55839995 | Common:1; Rare:79 | ||||
| chr12:55927763-55927800 | Rare:14 | ||||
| chr12:55931889-55932101 | Rare:51 |