| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:15097019-15097197 | Common:3; Rare:69 | ||||
| chr10:15097317-15097396 | Common:1; Rare:35 | ||||
| chr10:15860246-15860369 | Common:1; Rare:37 | ||||
| chr10:15860430-15860577 | Rare:44 | ||||
| chr10:16817316-16817678 | Common:5; Rare:124 | ||||
| chr10:17228734-17229026 | Common:3; Rare:75 | ||||
| chr10:17643898-17644315 | Common:2; Rare:128 | ||||
| chr10:18400987-18401057 | Rare:23 | ||||
| chr10:18659233-18659573 | Common:2; Rare:110 | ||||
| chr10:19816281-19816478 | Common:5; Rare:33 | ||||
| chr10:24466418-24466650 | Rare:38 | ||||
| chr10:27154315-27154480 | Rare:43 | ||||
| chr10:27154865-27155007 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chr10:27155218-27155391 | Common:4; Rare:63; Clinvar:2; Clinvar (benign):4 | ||||
| chr10:27240469-27240638 | Common:2; Rare:57 |