| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:50511654-50511782 | Common:1; Rare:19 | ||||
| chr10:50513117-50513342 | Rare:38 | ||||
| chr10:50542079-50542157 | Rare:12 | ||||
| chr10:50648800-50648881 | Common:2; Rare:18 | ||||
| chr10:50660142-50660298 | Common:4; Rare:43 | ||||
| chr10:52965292-52965426 | Rare:22 | ||||
| chr10:52965946-52966270 | Common:9; Rare:59 | ||||
| chr10:59036791-59037019 | Rare:42 | ||||
| chr10:59905088-59905394 | Common:1; Rare:52 | ||||
| chr10:59908541-59908627 | Common:1; Rare:21 | ||||
| chr10:60074315-60074866 | Common:2; Rare:116; Clinvar:7; Clinvar (benign):1 | ||||
| chr10:61286722-61286966 | Common:2; Rare:46 | ||||
| chr10:61897090-61897209 | Rare:21 | ||||
| chr10:61899979-61900202 | Rare:43 | ||||
| chr10:61900365-61900769 | Rare:75 |