| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:122112760-122113181 | Common:5; Rare:126 | ||||
| chr10:122163218-122163545 | Common:3; Rare:80 | ||||
| chr10:122191932-122192578 | Common:11; Rare:217 | ||||
| chr10:122374411-122374738 | Common:2; Rare:94 | ||||
| chr10:122374943-122375370 | Common:3; Rare:190 | ||||
| chr10:122461270-122462190 | Common:7; Rare:260; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr10:122954168-122954499 | Rare:121 | ||||
| chr10:122980308-122980434 | Common:1; Rare:15 | ||||
| chr10:122980626-122980771 | Common:2; Rare:57 | ||||
| chr10:123008671-123009061 | Common:6; Rare:109; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:123154188-123154454 | Common:1; Rare:87 | ||||
| chr10:124092320-124092820 | Common:3; Rare:112 | ||||
| chr10:124092840-124093210 | Common:2; Rare:74 | ||||
| chr10:124418911-124419110 | Common:4; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:124461700-124461864 | Common:5; Rare:59 |