| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6606415-6606548 | Common:2; Rare:55 | ||||
| chr12:6607300-6607678 | Common:5; Rare:77 | ||||
| chr12:6663079-6663380 | Common:1; Rare:87 | ||||
| chr12:6688879-6689232 | Rare:108 | ||||
| chr12:6689409-6689756 | Common:2; Rare:94 | ||||
| chr12:6723846-6724303 | Common:2; Rare:98 | ||||
| chr12:6752949-6753189 | Common:6; Rare:76 | ||||
| chr12:6765355-6765580 | Common:1; Rare:40 | ||||
| chr12:6851236-6851461 | Rare:54 | ||||
| chr12:6851879-6852182 | Rare:81 | ||||
| chr12:6867384-6867604 | Common:2; Rare:114; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873334-6873604 | Common:2; Rare:71 | ||||
| chr12:6904664-6905063 | Common:2; Rare:91 | ||||
| chr12:6914400-6914659 | Common:2; Rare:68 | ||||
| chr12:6943523-6943864 | Common:6; Rare:179 |