| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:118341600-118342080 | Rare:86 | ||||
| chr10:118342230-118342536 | Common:2; Rare:75 | ||||
| chr10:118754925-118755352 | Common:2; Rare:140 | ||||
| chr10:119029505-119029719 | Rare:85 | ||||
| chr10:119030001-119030401 | Common:5; Rare:194; Clinvar (pathogenic):2 | ||||
| chr10:119080778-119080984 | Common:1; Rare:89 | ||||
| chr10:119103859-119104171 | Common:2; Rare:71 | ||||
| chr10:119165260-119165550 | Common:2; Rare:75 | ||||
| chr10:119165570-119165900 | Common:2; Rare:122; Clinvar:1; Clinvar (benign):5 | ||||
| chr10:119178428-119178639 | Common:1; Rare:57 | ||||
| chr10:119178760-119179063 | Common:3; Rare:103 | ||||
| chr10:119207322-119207571 | Common:1; Rare:81 | ||||
| chr10:119542660-119542859 | Common:3; Rare:66 | ||||
| chr10:119596520-119596850 | Common:1; Rare:80 | ||||
| chr10:119596897-119597341 | Common:3; Rare:117 |