| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6493784-6494132 | Common:2; Rare:106 | ||||
| chr12:6534270-6534578 | Common:5; Rare:128 | ||||
| chr12:6568253-6568382 | Rare:48 | ||||
| chr12:6689445-6689750 | Common:2; Rare:78 | ||||
| chr12:6723970-6724170 | Rare:52 | ||||
| chr12:6752967-6753167 | Common:5; Rare:62 | ||||
| chr12:6851877-6852174 | Rare:78 | ||||
| chr12:6867381-6867561 | Common:2; Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6870119-6870430 | Common:1; Rare:96; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6904665-6904839 | Rare:41 | ||||
| chr12:6943537-6944124 | Common:17; Rare:450; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:6970621-6970964 | Common:4; Rare:107; Clinvar (benign):1 | ||||
| chr12:7108497-7108513 | Rare:5 | ||||
| chr12:7109235-7109267 | Rare:9 | ||||
| chr12:8697794-8698043 | Rare:103 |