| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:122375181-122375254 | Rare:22 | ||||
| chr10:122879531-122879914 | Common:4; Rare:92 | ||||
| chr10:122954186-122954486 | Rare:111 | ||||
| chr10:122980396-122980439 | Common:1; Rare:8 | ||||
| chr10:123008782-123009028 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124092369-124092527 | Rare:44 | ||||
| chr10:124093526-124093681 | Common:2; Rare:27 | ||||
| chr10:124418881-124419092 | Common:4; Rare:98; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:124461805-124461882 | Common:2; Rare:43 | ||||
| chr10:124791796-124791941 | Common:1; Rare:75 | ||||
| chr10:125719462-125719757 | Common:1; Rare:104 | ||||
| chr10:125823200-125823616 | Common:1; Rare:149; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125896443-125896628 | Common:5; Rare:19 | ||||
| chr10:126905297-126905473 | Rare:69 | ||||
| chr10:128047439-128047664 | Common:4; Rare:79 |