| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49623239-49623580 | Common:2; Rare:99 | ||||
| chr12:49706325-49707048 | Common:5; Rare:216 | ||||
| chr12:49707300-49707860 | Common:2; Rare:158 | ||||
| chr12:49741202-49741626 | Rare:124 | ||||
| chr12:49742000-49742110 | Rare:29 | ||||
| chr12:49827730-49828240 | Common:6; Rare:120 | ||||
| chr12:49828260-49828690 | Common:1; Rare:125 | ||||
| chr12:49842700-49843000 | Common:2; Rare:72 | ||||
| chr12:49843063-49843238 | Common:2; Rare:66; Clinvar (benign):1 | ||||
| chr12:49903850-49904150 | Common:2; Rare:77 | ||||
| chr12:50025402-50025795 | Common:2; Rare:110 | ||||
| chr12:50085018-50085397 | Common:1; Rare:100 | ||||
| chr12:50085404-50086060 | Common:7; Rare:180 | ||||
| chr12:50112157-50112278 | Common:1; Rare:32 | ||||
| chr12:50167248-50167769 | Common:3; Rare:133 |