| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:122112827-122113078 | Common:3; Rare:81 | ||||
| chr10:122879570-122879720 | Common:3; Rare:35 | ||||
| chr10:122954155-122954508 | Common:1; Rare:133 | ||||
| chr10:122980294-122980492 | Common:1; Rare:48 | ||||
| chr10:123008791-123009028 | Common:5; Rare:66; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124418902-124419092 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:124791736-124791938 | Common:1; Rare:105 | ||||
| chr10:124801742-124801835 | Rare:33 | ||||
| chr10:125160997-125161281 | Common:4; Rare:103 | ||||
| chr10:125719429-125719802 | Common:1; Rare:144 | ||||
| chr10:125823185-125823594 | Common:2; Rare:147; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:125896282-125896630 | Common:5; Rare:30 | ||||
| chr10:126905275-126905465 | Rare:72 | ||||
| chr10:128047421-128047628 | Common:2; Rare:66 | ||||
| chr10:128126351-128126627 | Common:2; Rare:80 |