| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101588138-101588335 | Rare:81 | ||||
| chr10:102394336-102394536 | Rare:57 | ||||
| chr10:102714262-102714636 | Common:2; Rare:126 | ||||
| chr10:103396408-103396737 | Rare:112 | ||||
| chr10:103967018-103967179 | Common:1; Rare:42 | ||||
| chr10:104338403-104338549 | Rare:36 | ||||
| chr10:110006005-110006106 | Common:2; Rare:26 | ||||
| chr10:110007810-110008016 | Rare:53 | ||||
| chr10:110497737-110497907 | Common:5; Rare:55 | ||||
| chr10:110919118-110919654 | Common:8; Rare:141; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:112446725-112447277 | Common:3; Rare:131 | ||||
| chr10:112950560-112950686 | Common:2; Rare:19 | ||||
| chr10:113854171-113854873 | Common:1; Rare:152 | ||||
| chr10:118046686-118047013 | Common:4; Rare:107 | ||||
| chr10:119080636-119080950 | Common:4; Rare:109 |