| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:67838037-67838308 | Common:2; Rare:51 | ||||
| chr10:68075193-68075474 | Common:4; Rare:120 | ||||
| chr10:68331907-68332111 | Common:1; Rare:90 | ||||
| chr10:68332920-68332986 | Rare:17 | ||||
| chr10:68407252-68407382 | Common:3; Rare:40 | ||||
| chr10:68721422-68721534 | Common:2; Rare:35 | ||||
| chr10:68901050-68901346 | Common:3; Rare:118 | ||||
| chr10:68956100-68956231 | Rare:61 | ||||
| chr10:69087974-69088113 | Rare:23 | ||||
| chr10:70146647-70146869 | Common:1; Rare:58 | ||||
| chr10:70170457-70170719 | Common:3; Rare:85 | ||||
| chr10:70233323-70233563 | Common:6; Rare:86; Clinvar (benign):1 | ||||
| chr10:70403971-70404149 | Rare:68 | ||||
| chr10:70815812-70815996 | Rare:70 | ||||
| chr10:70888536-70888680 | Common:2; Rare:43; Clinvar:5; Clinvar (benign):2 |