| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17643834-17644301 | Common:2; Rare:152 | ||||
| chr10:18140121-18140435 | Common:3; Rare:71 | ||||
| chr10:18140506-18140895 | Common:2; Rare:137; Clinvar:5; Clinvar (benign):9 | ||||
| chr10:18140914-18141094 | Common:2; Rare:37 | ||||
| chr10:18141443-18141713 | Common:2; Rare:40 | ||||
| chr10:18651523-18651730 | Common:1; Rare:82 | ||||
| chr10:18658941-18659019 | Common:1; Rare:22 | ||||
| chr10:18659051-18659596 | Common:4; Rare:168 | ||||
| chr10:19488979-19489105 | Common:3; Rare:63 | ||||
| chr10:19815798-19815881 | Rare:26 | ||||
| chr10:19815974-19816474 | Common:7; Rare:114 | ||||
| chr10:19816512-19816710 | Rare:48 | ||||
| chr10:21174050-21174202 | Rare:40 | ||||
| chr10:21174213-21174591 | Common:1; Rare:96 | ||||
| chr10:21496554-21496873 | Common:1; Rare:106 |