| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:121974690-121974897 | Common:2; Rare:62 | ||||
| chr10:122019187-122019378 | Rare:36 | ||||
| chr10:122879541-122879623 | Common:1; Rare:27 | ||||
| chr10:122954185-122954508 | Common:1; Rare:119 | ||||
| chr10:123008782-123009047 | Common:5; Rare:79; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124418911-124419092 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125719433-125719761 | Common:1; Rare:118 | ||||
| chr10:125823103-125823573 | Common:2; Rare:161; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:125896447-125896607 | Common:2; Rare:12 | ||||
| chr10:126905297-126905465 | Rare:64 | ||||
| chr10:128047458-128047619 | Common:2; Rare:49 | ||||
| chr10:131981837-131982133 | Common:4; Rare:108 | ||||
| chr10:132331821-132332240 | Common:13; Rare:136 | ||||
| chr10:132942549-132942621 | Common:1; Rare:18 | ||||
| chr10:133308835-133308980 | Rare:68 |