| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:72216254-72216528 | Common:3; Rare:81 | ||||
| chr10:72273698-72273942 | Rare:66 | ||||
| chr10:72354877-72355196 | Common:2; Rare:114 | ||||
| chr10:73096804-73097033 | Common:3; Rare:69 | ||||
| chr10:73167970-73168252 | Rare:73 | ||||
| chr10:73252559-73252789 | Common:2; Rare:66; Clinvar:5; Clinvar (benign):2 | ||||
| chr10:73495599-73495757 | Rare:31 | ||||
| chr10:73625983-73626118 | Rare:25 | ||||
| chr10:73744251-73744424 | Common:1; Rare:47 | ||||
| chr10:73772905-73773141 | Rare:82 | ||||
| chr10:74151048-74151235 | Common:1; Rare:50 | ||||
| chr10:74176521-74176816 | Rare:72; Clinvar:3 | ||||
| chr10:75111353-75111698 | Common:1; Rare:96 | ||||
| chr10:75210492-75210867 | Common:1; Rare:127 | ||||
| chr10:78029468-78029651 | Common:1; Rare:54; Clinvar (benign):1 |