| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4649045-4649144 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr12:6200005-6200480 | Common:4; Rare:138 | ||||
| chr12:6375334-6375462 | Rare:21 | ||||
| chr12:6383988-6384245 | Common:1; Rare:55 | ||||
| chr12:6384787-6385051 | Common:1; Rare:58 | ||||
| chr12:6452084-6452170 | Rare:18 | ||||
| chr12:6493140-6493381 | Common:7; Rare:75 | ||||
| chr12:6493778-6494135 | Common:2; Rare:107 | ||||
| chr12:6536532-6536788 | Rare:90 | ||||
| chr12:6568273-6568382 | Rare:40 | ||||
| chr12:6606300-6606556 | Common:3; Rare:110 | ||||
| chr12:6663100-6663403 | Common:2; Rare:84 | ||||
| chr12:6688884-6689144 | Rare:83 | ||||
| chr12:6723852-6724152 | Common:1; Rare:59 | ||||
| chr12:6766310-6766736 | Rare:127 |