| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119651155-119651468 | Common:7; Rare:114; Clinvar:1; Clinvar (benign):4 | ||||
| chr10:119725716-119726172 | Common:4; Rare:155 | ||||
| chr10:119872778-119873197 | Common:4; Rare:139 | ||||
| chr10:119892447-119892860 | Common:3; Rare:147 | ||||
| chr10:120851150-120851450 | Common:5; Rare:109 | ||||
| chr10:120851534-120851755 | Rare:56 | ||||
| chr10:121927366-121927629 | Rare:51 | ||||
| chr10:121927930-121928317 | Common:2; Rare:116 | ||||
| chr10:121974742-121974966 | Common:1; Rare:67 | ||||
| chr10:121975078-121975361 | Common:1; Rare:69 | ||||
| chr10:122879519-122879836 | Common:4; Rare:76 | ||||
| chr10:122879896-122880036 | Rare:36 | ||||
| chr10:122954134-122954320 | Rare:66 | ||||
| chr10:122980287-122980511 | Common:2; Rare:54 | ||||
| chr10:122980523-122980864 | Common:3; Rare:120 |