| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:89327842-89328017 | Common:1; Rare:24 | ||||
| chr10:89392383-89392659 | Common:7; Rare:67 | ||||
| chr10:89414680-89414785 | Common:3; Rare:50 | ||||
| chr10:89701424-89701646 | Common:1; Rare:64 | ||||
| chr10:91923716-91923811 | Rare:36 | ||||
| chr10:92291022-92291469 | Common:6; Rare:141 | ||||
| chr10:92574013-92574148 | Common:1; Rare:41 | ||||
| chr10:92592972-92593169 | Common:3; Rare:60 | ||||
| chr10:95290822-95291186 | Common:2; Rare:142 | ||||
| chr10:95561338-95561632 | Common:4; Rare:92 | ||||
| chr10:95693891-95694207 | Common:5; Rare:98; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:95907865-95907938 | Common:1; Rare:22 | ||||
| chr10:97426082-97426257 | Common:2; Rare:63 | ||||
| chr10:97445969-97446209 | Common:1; Rare:63 | ||||
| chr10:97687223-97687627 | Common:5; Rare:116 |