| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:21604033-21604338 | Common:6; Rare:147 | ||||
| chr13:21670897-21671163 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:21674246-21674501 | Common:3; Rare:56 | ||||
| chr13:23570216-23570570 | Common:2; Rare:72 | ||||
| chr13:23570586-23570861 | Common:1; Rare:54 | ||||
| chr13:23578785-23579004 | Common:1; Rare:58 | ||||
| chr13:23579148-23579485 | Common:6; Rare:112 | ||||
| chr13:23579573-23579735 | Common:1; Rare:39 | ||||
| chr13:23579805-23579878 | Common:1; Rare:15 | ||||
| chr13:23888766-23888929 | Common:1; Rare:41 | ||||
| chr13:23889130-23889586 | Common:1; Rare:148 | ||||
| chr13:23979633-23979800 | Common:2; Rare:35 | ||||
| chr13:23980232-23980420 | Common:1; Rare:57 | ||||
| chr13:24160537-24160832 | Common:1; Rare:81 | ||||
| chr13:24160875-24160940 | Rare:16 |