| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49269401-49269975 | Common:4; Rare:226 | ||||
| chr12:49297470-49297740 | Common:6; Rare:171; Clinvar:6 | ||||
| chr12:49322912-49323344 | Common:8; Rare:212 | ||||
| chr12:49366680-49367010 | Common:2; Rare:139 | ||||
| chr12:49367110-49367583 | Common:3; Rare:246 | ||||
| chr12:49567842-49568495 | Common:4; Rare:220 | ||||
| chr12:49623239-49623580 | Common:3; Rare:155 | ||||
| chr12:49707403-49707742 | Common:2; Rare:98 | ||||
| chr12:49741216-49741614 | Rare:218 | ||||
| chr12:49758140-49758901 | Common:10; Rare:292 | ||||
| chr12:49828390-49828667 | Common:1; Rare:137 | ||||
| chr12:49843054-49843248 | Common:3; Rare:122; Clinvar (benign):1 | ||||
| chr12:49962898-49963133 | Common:1; Rare:23 | ||||
| chr12:50025336-50025747 | Common:4; Rare:202 | ||||
| chr12:50070450-50070800 | Common:5; Rare:108 |