| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:26222246-26222377 | Common:2; Rare:38 | ||||
| chr13:27251235-27251626 | Common:8; Rare:121 | ||||
| chr13:27270696-27270843 | Rare:51 | ||||
| chr13:27424526-27424740 | Common:2; Rare:69 | ||||
| chr13:27450119-27450222 | Common:3; Rare:32 | ||||
| chr13:27450383-27450620 | Common:4; Rare:96 | ||||
| chr13:27620400-27620888 | Common:4; Rare:166 | ||||
| chr13:28138147-28138255 | Common:1; Rare:33 | ||||
| chr13:28138596-28138910 | Common:4; Rare:80 | ||||
| chr13:28138919-28138982 | Rare:18 | ||||
| chr13:28658937-28659001 | Rare:15 | ||||
| chr13:28659066-28659194 | Rare:55; Clinvar (pathogenic):1 | ||||
| chr13:28718775-28719166 | Common:1; Rare:104 | ||||
| chr13:29849908-29850226 | Common:1; Rare:95 | ||||
| chr13:29850286-29850478 | Common:3; Rare:54 |