| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:110919143-110919321 | Common:1; Rare:42 | ||||
| chr10:110919353-110919647 | Common:7; Rare:80; Clinvar:1 | ||||
| chr10:112183707-112183851 | Common:3; Rare:54 | ||||
| chr10:112376150-112376255 | Rare:13 | ||||
| chr10:112446901-112447320 | Common:3; Rare:103 | ||||
| chr10:113854591-113854666 | Rare:18 | ||||
| chr10:118754909-118755305 | Common:1; Rare:129 | ||||
| chr10:119080638-119080972 | Common:5; Rare:121 | ||||
| chr10:119872821-119873094 | Common:4; Rare:98 | ||||
| chr10:120851307-120851439 | Common:1; Rare:58 | ||||
| chr10:120851597-120851784 | Common:1; Rare:44 | ||||
| chr10:121928003-121928169 | Common:1; Rare:31 | ||||
| chr10:122879540-122879687 | Common:3; Rare:43 | ||||
| chr10:122954192-122954458 | Rare:97 | ||||
| chr10:123008703-123009035 | Common:6; Rare:88; Clinvar:4; Clinvar (benign):5 |