| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6851887-6852174 | Rare:73 | ||||
| chr12:6873317-6873541 | Common:1; Rare:64 | ||||
| chr12:6943938-6944172 | Common:5; Rare:235; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970628-6970977 | Common:4; Rare:113; Clinvar (benign):1 | ||||
| chr12:7018468-7018732 | Common:1; Rare:72 | ||||
| chr12:7108365-7108681 | Common:2; Rare:99 | ||||
| chr12:7109126-7109567 | Common:2; Rare:108 | ||||
| chr12:7130264-7130423 | Common:4; Rare:43 | ||||
| chr12:7751616-7751778 | Common:2; Rare:59 | ||||
| chr12:8032568-8032777 | Common:4; Rare:70 | ||||
| chr12:8697827-8698148 | Common:2; Rare:111 | ||||
| chr12:8914368-8914764 | Common:6; Rare:115 | ||||
| chr12:8949975-8950119 | Common:1; Rare:37 | ||||
| chr12:9079744-9079950 | Rare:45 | ||||
| chr12:9091411-9091565 | Common:1; Rare:34 |