| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:70146540-70146934 | Common:3; Rare:273 | ||||
| chr10:70170430-70170834 | Common:10; Rare:314 | ||||
| chr10:70233245-70233738 | Common:17; Rare:326; Clinvar (benign):2 | ||||
| chr10:70382494-70382869 | Common:15; Rare:321 | ||||
| chr10:70403939-70404218 | Common:1; Rare:193 | ||||
| chr10:70672090-70672630 | Common:5; Rare:130 | ||||
| chr10:70815801-70816143 | Rare:207 | ||||
| chr10:70816140-70816990 | Common:3; Rare:360 | ||||
| chr10:70887730-70888068 | Common:4; Rare:128 | ||||
| chr10:70888060-70888380 | Common:9; Rare:147 | ||||
| chr10:70888489-70888692 | Common:4; Rare:114; Clinvar:10; Clinvar (benign):4 | ||||
| chr10:71212367-71212659 | Common:1; Rare:85 | ||||
| chr10:71319034-71319370 | Common:6; Rare:170; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:71319530-71319910 | Common:8; Rare:148 | ||||
| chr10:71851174-71851512 | Common:15; Rare:363; Clinvar:12; Clinvar (benign):24; Clinvar (pathogenic):3 |