| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119178758-119179021 | Common:3; Rare:97 | ||||
| chr10:119651237-119651392 | Common:4; Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:119725781-119726082 | Common:3; Rare:100 | ||||
| chr10:119818482-119818731 | Rare:84 | ||||
| chr10:119892548-119892785 | Common:3; Rare:90 | ||||
| chr10:120851162-120851336 | Common:4; Rare:52 | ||||
| chr10:120851338-120851445 | Common:1; Rare:47 | ||||
| chr10:121927977-121928068 | Rare:31 | ||||
| chr10:121974752-121974872 | Common:1; Rare:42 | ||||
| chr10:122112626-122112929 | Common:4; Rare:91 | ||||
| chr10:122375140-122375245 | Common:1; Rare:38 | ||||
| chr10:122879538-122879677 | Common:3; Rare:39 | ||||
| chr10:122954185-122954496 | Rare:113 | ||||
| chr10:122980356-122980431 | Common:1; Rare:10 | ||||
| chr10:123008776-123009035 | Common:5; Rare:71; Clinvar:4; Clinvar (benign):5 |