| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:121596665-121596924 | Common:1; Rare:54 | ||||
| chr10:121927890-121928079 | Common:1; Rare:71 | ||||
| chr10:121928436-121928541 | Rare:27 | ||||
| chr10:122879516-122879691 | Common:3; Rare:49 | ||||
| chr10:122954182-122954516 | Common:1; Rare:121 | ||||
| chr10:122980344-122980473 | Common:1; Rare:33 | ||||
| chr10:123008791-123009011 | Common:5; Rare:60; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124092373-124092567 | Common:1; Rare:51 | ||||
| chr10:124093483-124093681 | Common:2; Rare:35 | ||||
| chr10:124418892-124419103 | Common:5; Rare:96; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:124461766-124461873 | Common:3; Rare:48 | ||||
| chr10:124791745-124791933 | Common:1; Rare:102 | ||||
| chr10:124801735-124801830 | Rare:33 | ||||
| chr10:125719456-125719780 | Common:1; Rare:122 | ||||
| chr10:125823159-125823666 | Common:2; Rare:183; Clinvar:1; Clinvar (benign):2 |