| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:69087930-69088234 | Rare:65 | ||||
| chr10:69179943-69180291 | Common:1; Rare:108 | ||||
| chr10:69451313-69451593 | Common:2; Rare:79 | ||||
| chr10:70233348-70233563 | Common:5; Rare:75 | ||||
| chr10:71773494-71773704 | Common:3; Rare:64 | ||||
| chr10:71819464-71819892 | Common:1; Rare:170; Clinvar:5; Clinvar (benign):3 | ||||
| chr10:71851187-71851334 | Common:3; Rare:72; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr10:71964116-71964239 | Common:1; Rare:40 | ||||
| chr10:71964302-71964556 | Common:4; Rare:67; Clinvar:1; Clinvar (benign):3 | ||||
| chr10:72216237-72216523 | Common:3; Rare:84 | ||||
| chr10:72273662-72273988 | Rare:97 | ||||
| chr10:72354953-72355296 | Common:2; Rare:98 | ||||
| chr10:73096804-73097138 | Common:4; Rare:95 | ||||
| chr10:73167941-73168353 | Rare:123 | ||||
| chr10:73252575-73252802 | Common:2; Rare:63; Clinvar:4; Clinvar (benign):2 |