| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:122112719-122113106 | Common:4; Rare:118 | ||||
| chr10:122374422-122374784 | Common:2; Rare:114 | ||||
| chr10:122375134-122375235 | Common:1; Rare:38 | ||||
| chr10:122954174-122954479 | Rare:109 | ||||
| chr10:123008791-123009032 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124092369-124092598 | Common:1; Rare:57 | ||||
| chr10:124093498-124093665 | Common:2; Rare:32 | ||||
| chr10:124418892-124419092 | Common:4; Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:124461715-124461865 | Common:4; Rare:53 | ||||
| chr10:124791735-124791993 | Common:2; Rare:134 | ||||
| chr10:125719453-125719755 | Common:1; Rare:107 | ||||
| chr10:125823192-125823568 | Common:1; Rare:125; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125881279-125881451 | Common:1; Rare:42 | ||||
| chr10:125896462-125896568 | Common:1; Rare:4 | ||||
| chr10:126905255-126905473 | Rare:86 |