| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53252053-53252217 | Common:3; Rare:59 | ||||
| chr12:53501213-53501352 | Rare:35 | ||||
| chr12:53501537-53501660 | Rare:30 | ||||
| chr12:54419449-54419662 | Rare:36 | ||||
| chr12:55681861-55681959 | Rare:30 | ||||
| chr12:55682056-55682252 | Common:2; Rare:57 | ||||
| chr12:55688920-55689142 | Common:2; Rare:54; Clinvar:3 | ||||
| chr12:55707495-55707527 | Rare:8; Clinvar:2 | ||||
| chr12:55707536-55707655 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):4 | ||||
| chr12:55707685-55707953 | Common:1; Rare:62; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:55712063-55712439 | Common:7; Rare:90; Clinvar (benign):1 | ||||
| chr12:55715986-55716192 | Common:2; Rare:93 | ||||
| chr12:55720343-55720411 | Common:1; Rare:12; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:55725840-55726258 | Rare:95 | ||||
| chr12:55728275-55728521 | Rare:77 |