| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95942460-95942647 | Common:3; Rare:45 | ||||
| chr12:95942810-95943340 | Common:5; Rare:168 | ||||
| chr12:95943370-95943670 | Common:5; Rare:119 | ||||
| chr12:96035401-96036001 | Common:9; Rare:317 | ||||
| chr12:96193702-96194028 | Rare:70 | ||||
| chr12:96194239-96194579 | Common:7; Rare:163 | ||||
| chr12:96399241-96400072 | Common:6; Rare:523 | ||||
| chr12:96400042-96400242 | Common:1; Rare:50 | ||||
| chr12:96400172-96400665 | Common:6; Rare:403 | ||||
| chr12:96907103-96907366 | Common:5; Rare:231 | ||||
| chr12:98515282-98516080 | Common:2; Rare:641; Clinvar:23; Clinvar (benign):6 | ||||
| chr12:98516253-98516623 | Common:6; Rare:199 | ||||
| chr12:98593376-98593797 | Common:6; Rare:347; Clinvar:12; Clinvar (benign):12 | ||||
| chr12:98644681-98644918 | Common:9; Rare:179 | ||||
| chr12:98644947-98645406 | Common:7; Rare:311 |