| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:74825238-74825589 | Rare:92 | ||||
| chr10:74825821-74825955 | Rare:31 | ||||
| chr10:74826095-74826658 | Common:2; Rare:136; Clinvar (benign):2 | ||||
| chr10:75099902-75100302 | Common:1; Rare:119 | ||||
| chr10:75111251-75111352 | Rare:23 | ||||
| chr10:75111353-75111719 | Common:1; Rare:104 | ||||
| chr10:75209881-75210307 | Common:5; Rare:159 | ||||
| chr10:75210369-75210847 | Common:1; Rare:171 | ||||
| chr10:75235506-75235913 | Common:3; Rare:179 | ||||
| chr10:75401727-75401989 | Common:2; Rare:95 | ||||
| chr10:75402224-75402710 | Common:4; Rare:220 | ||||
| chr10:77637221-77637621 | Common:3; Rare:209; Clinvar:12; Clinvar (benign):3 | ||||
| chr10:77637707-77638031 | Common:4; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:77926920-77927450 | Common:3; Rare:143 | ||||
| chr10:78029502-78029663 | Common:1; Rare:41; Clinvar (benign):1 |