| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:117005358-117005407 | Rare:12 | ||||
| chr10:117126421-117126785 | Common:1; Rare:23 | ||||
| chr10:117374410-117374784 | Common:2; Rare:99 | ||||
| chr10:117374797-117374967 | Common:1; Rare:56 | ||||
| chr10:117375304-117375550 | Common:3; Rare:82 | ||||
| chr10:118046030-118046493 | Common:1; Rare:127 | ||||
| chr10:118046575-118047033 | Common:4; Rare:145 | ||||
| chr10:118342233-118342409 | Common:2; Rare:45 | ||||
| chr10:118754515-118754626 | Rare:47 | ||||
| chr10:118754832-118755345 | Common:2; Rare:172 | ||||
| chr10:119080502-119080938 | Common:4; Rare:143 | ||||
| chr10:119165362-119165766 | Common:4; Rare:142; Clinvar:1; Clinvar (benign):5 | ||||
| chr10:119178531-119178588 | Common:1; Rare:17 | ||||
| chr10:119178779-119178940 | Common:3; Rare:64 | ||||
| chr10:119596960-119597123 | Rare:41 |