| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119651209-119651440 | Common:6; Rare:93; Clinvar:1; Clinvar (benign):4 | ||||
| chr10:119726023-119726267 | Common:2; Rare:96 | ||||
| chr10:119872800-119873050 | Common:4; Rare:91 | ||||
| chr10:119892517-119892837 | Common:3; Rare:124 | ||||
| chr10:120851185-120851483 | Common:6; Rare:107 | ||||
| chr10:121927863-121928208 | Common:2; Rare:105 | ||||
| chr10:121928429-121928559 | Rare:36 | ||||
| chr10:121974768-121974891 | Rare:46 | ||||
| chr10:121975126-121975376 | Common:1; Rare:52 | ||||
| chr10:122461408-122461632 | Common:1; Rare:56; Clinvar (benign):1 | ||||
| chr10:122879488-122879719 | Common:3; Rare:63 | ||||
| chr10:122954156-122954506 | Common:1; Rare:131 | ||||
| chr10:123008692-123009044 | Common:6; Rare:96; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124791726-124791938 | Common:1; Rare:112 | ||||
| chr10:124801733-124801863 | Rare:46 |