| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57633101-57633250 | Rare:47 | ||||
| chr12:57693845-57694195 | Common:1; Rare:98 | ||||
| chr12:57744842-57745096 | Common:1; Rare:54 | ||||
| chr12:57745246-57745427 | Common:1; Rare:40 | ||||
| chr12:57752220-57752700 | Common:1; Rare:127; Clinvar:1 | ||||
| chr12:57772079-57772311 | Rare:69 | ||||
| chr12:57941360-57941740 | Common:3; Rare:116 | ||||
| chr12:58920139-58920308 | Common:1; Rare:53 | ||||
| chr12:58920541-58920693 | Common:2; Rare:48 | ||||
| chr12:59595895-59596176 | Common:5; Rare:71 | ||||
| chr12:62191664-62191942 | Rare:59 | ||||
| chr12:62260048-62260441 | Common:1; Rare:148 | ||||
| chr12:62466612-62466838 | Rare:70 | ||||
| chr12:63780087-63780175 | Rare:41; Clinvar (pathogenic):1 | ||||
| chr12:64222241-64222346 | Rare:36 |