| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119165643-119165766 | Rare:57; Clinvar (benign):3 | ||||
| chr10:119178769-119178862 | Common:1; Rare:42 | ||||
| chr10:119596935-119597345 | Common:2; Rare:110 | ||||
| chr10:119651228-119651412 | Common:6; Rare:69; Clinvar:1; Clinvar (benign):4 | ||||
| chr10:119818510-119818731 | Rare:75 | ||||
| chr10:119892519-119892789 | Common:3; Rare:100 | ||||
| chr10:120851258-120851411 | Common:3; Rare:57 | ||||
| chr10:121927939-121928068 | Common:1; Rare:51 | ||||
| chr10:121928418-121928551 | Rare:39 | ||||
| chr10:121974767-121974881 | Rare:43 | ||||
| chr10:122112718-122113122 | Common:4; Rare:124 | ||||
| chr10:122954185-122954508 | Common:1; Rare:119 | ||||
| chr10:122980341-122980482 | Common:1; Rare:38 | ||||
| chr10:123008782-123009045 | Common:5; Rare:78; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124092365-124092623 | Common:1; Rare:63 |