| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119651135-119651457 | Common:7; Rare:119; Clinvar:1; Clinvar (benign):4 | ||||
| chr10:119725719-119726155 | Common:4; Rare:151 | ||||
| chr10:119726278-119726507 | Common:2; Rare:65 | ||||
| chr10:119872822-119873124 | Common:4; Rare:110 | ||||
| chr10:119873244-119873644 | Common:3; Rare:170 | ||||
| chr10:119892455-119892783 | Common:3; Rare:116 | ||||
| chr10:120851078-120851410 | Common:8; Rare:98 | ||||
| chr10:121595980-121596330 | Common:2; Rare:61 | ||||
| chr10:121596917-121597099 | Common:1; Rare:38 | ||||
| chr10:121598421-121598660 | Common:2; Rare:82; Clinvar:1 | ||||
| chr10:121598679-121598877 | Common:3; Rare:40 | ||||
| chr10:121927880-121928222 | Common:2; Rare:104 | ||||
| chr10:121928390-121928650 | Common:1; Rare:69 | ||||
| chr10:121974753-121974908 | Common:1; Rare:49 | ||||
| chr10:121975132-121975386 | Common:1; Rare:52 |