| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:122954182-122954464 | Rare:102 | ||||
| chr10:123008791-123009023 | Common:5; Rare:63; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124092369-124092598 | Common:1; Rare:57 | ||||
| chr10:124418888-124419092 | Common:4; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:124461726-124461868 | Common:4; Rare:53 | ||||
| chr10:124791790-124791938 | Common:1; Rare:78 | ||||
| chr10:124801735-124801846 | Rare:36 | ||||
| chr10:125719453-125719761 | Common:1; Rare:109 | ||||
| chr10:125823184-125823611 | Common:2; Rare:152; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:125896474-125896589 | Rare:4 | ||||
| chr10:126905302-126905474 | Rare:67 | ||||
| chr10:127906940-127907217 | Common:3; Rare:78 | ||||
| chr10:127987062-127987291 | Common:2; Rare:45 | ||||
| chr10:128047411-128047664 | Common:4; Rare:88 | ||||
| chr10:129466966-129467273 | Common:3; Rare:120 |