| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102055820-102056058 | Common:2; Rare:114 | ||||
| chr10:102056066-102056410 | Common:7; Rare:227 | ||||
| chr10:102065153-102065547 | Common:3; Rare:235 | ||||
| chr10:102065591-102066480 | Common:9; Rare:356; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr10:102114420-102114730 | Rare:148 | ||||
| chr10:102114879-102115141 | Common:8; Rare:174 | ||||
| chr10:102120245-102120726 | Common:6; Rare:404 | ||||
| chr10:102132837-102133222 | Common:3; Rare:196 | ||||
| chr10:102133480-102133820 | Common:2; Rare:136 | ||||
| chr10:102151901-102152470 | Common:9; Rare:310 | ||||
| chr10:102226069-102226382 | Common:4; Rare:152 | ||||
| chr10:102245093-102245635 | Common:3; Rare:186 | ||||
| chr10:102393900-102394167 | Common:2; Rare:132 | ||||
| chr10:102394264-102394586 | Common:2; Rare:223 | ||||
| chr10:102395531-102395809 | Common:3; Rare:175 |