| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17229061-17229339 | Common:2; Rare:53 | ||||
| chr10:17643894-17644241 | Common:2; Rare:103 | ||||
| chr10:18651540-18651738 | Common:1; Rare:82 | ||||
| chr10:18659226-18659506 | Common:2; Rare:97 | ||||
| chr10:19816204-19816432 | Common:5; Rare:52 | ||||
| chr10:21524527-21524662 | Rare:27 | ||||
| chr10:22316272-22316456 | Rare:77 | ||||
| chr10:22927979-22928072 | Common:1; Rare:37 | ||||
| chr10:23694567-23694774 | Common:1; Rare:54 | ||||
| chr10:24722742-24722832 | Rare:32 | ||||
| chr10:26216272-26216431 | Common:1; Rare:40 | ||||
| chr10:26216677-26216783 | Common:1; Rare:31 | ||||
| chr10:27100427-27100582 | Common:3; Rare:48; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:27154323-27154448 | Rare:33 | ||||
| chr10:27155264-27155403 | Common:5; Rare:58; Clinvar:1; Clinvar (benign):5 |