| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:99659149-99659612 | Common:2; Rare:114 | ||||
| chr10:99731973-99732787 | Common:6; Rare:253; Clinvar:9; Clinvar (benign):3 | ||||
| chr10:99732875-99732896 | Rare:5 | ||||
| chr10:99782467-99782831 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:100009829-100010021 | Common:1; Rare:60 | ||||
| chr10:100081611-100081739 | Rare:22 | ||||
| chr10:100185527-100185598 | Rare:20 | ||||
| chr10:100185829-100186369 | Common:2; Rare:161 | ||||
| chr10:100228943-100229136 | Common:7; Rare:46 | ||||
| chr10:100229485-100229758 | Common:2; Rare:93 | ||||
| chr10:100267064-100267414 | Common:4; Rare:59 | ||||
| chr10:100267430-100267804 | Common:4; Rare:111 | ||||
| chr10:100286075-100286287 | Rare:54 | ||||
| chr10:100286589-100286800 | Common:5; Rare:106 | ||||
| chr10:100346486-100346677 | Common:3; Rare:43 |