| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4320949-4321260 | Common:5; Rare:118 | ||||
| chr12:4538436-4538786 | Rare:74 | ||||
| chr12:4649005-4649140 | Common:2; Rare:42; Clinvar (benign):1 | ||||
| chr12:5043692-5044034 | Common:4; Rare:78; Clinvar (benign):1 | ||||
| chr12:6200170-6200421 | Common:3; Rare:78 | ||||
| chr12:6341810-6342106 | Rare:61; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6383957-6384255 | Common:1; Rare:68 | ||||
| chr12:6444894-6444987 | Rare:18 | ||||
| chr12:6470605-6470985 | Common:3; Rare:119 | ||||
| chr12:6493203-6493386 | Common:6; Rare:50 | ||||
| chr12:6493778-6494132 | Common:2; Rare:107 | ||||
| chr12:6534431-6534860 | Common:8; Rare:183 | ||||
| chr12:6536491-6536818 | Rare:106 | ||||
| chr12:6548812-6548946 | Rare:46 | ||||
| chr12:6568224-6568384 | Rare:60 |