| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:98268229-98268433 | Common:1; Rare:56 | ||||
| chr10:99430622-99430936 | Common:3; Rare:70 | ||||
| chr10:99659256-99659529 | Common:1; Rare:68 | ||||
| chr10:99732076-99732332 | Rare:93; Clinvar:3 | ||||
| chr10:100185920-100186198 | Rare:107 | ||||
| chr10:100229562-100229629 | Rare:18 | ||||
| chr10:100267624-100267858 | Common:3; Rare:63 | ||||
| chr10:100912751-100912996 | Common:1; Rare:76 | ||||
| chr10:100913335-100913442 | Rare:28 | ||||
| chr10:100987445-100987571 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:101031111-101031292 | Common:1; Rare:40 | ||||
| chr10:101588211-101588329 | Rare:48 | ||||
| chr10:101818334-101818757 | Common:1; Rare:115 | ||||
| chr10:102056102-102056310 | Common:1; Rare:53 | ||||
| chr10:102114952-102115084 | Common:2; Rare:42 |