| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119651222-119651382 | Common:2; Rare:63 | ||||
| chr10:119725649-119725841 | Common:1; Rare:58 | ||||
| chr10:119726173-119726354 | Rare:57 | ||||
| chr10:119892548-119892777 | Common:3; Rare:87 | ||||
| chr10:120851189-120851498 | Common:6; Rare:112 | ||||
| chr10:121927945-121928093 | Rare:56 | ||||
| chr10:122112831-122113078 | Common:3; Rare:79 | ||||
| chr10:122879547-122879696 | Common:3; Rare:42 | ||||
| chr10:122954166-122954514 | Common:1; Rare:127 | ||||
| chr10:122980329-122980439 | Common:1; Rare:15 | ||||
| chr10:122980604-122980794 | Common:2; Rare:73 | ||||
| chr10:123008790-123009028 | Common:5; Rare:66; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124418894-124419092 | Common:4; Rare:89; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:124744048-124744090 | Rare:12 | ||||
| chr10:124791804-124791959 | Common:1; Rare:76 |