| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51217039-51217439 | Common:3; Rare:156 | ||||
| chr12:51217472-51217672 | Common:2; Rare:33 | ||||
| chr12:51217790-51218380 | Common:20; Rare:416 | ||||
| chr12:51238533-51238933 | Common:48; Rare:727 | ||||
| chr12:51239029-51239429 | Common:14; Rare:444 | ||||
| chr12:51269337-51270900 | Common:65; Rare:1704 | ||||
| chr12:51390647-51391047 | Common:2; Rare:125 | ||||
| chr12:51391181-51391929 | Common:20; Rare:706 | ||||
| chr12:51590640-51591000 | Common:3; Rare:168 | ||||
| chr12:51887829-51888229 | Common:7; Rare:254 | ||||
| chr12:51912100-51912430 | Common:4; Rare:191 | ||||
| chr12:51912405-51912805 | Common:4; Rare:153; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:51951270-51951771 | Common:18; Rare:635 | ||||
| chr12:52010080-52010590 | Rare:247 | ||||
| chr12:52022704-52023519 | Common:12; Rare:425 |