| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:18651504-18651977 | Common:2; Rare:146 | ||||
| chr10:18659233-18659536 | Common:2; Rare:99 | ||||
| chr10:18659577-18659666 | Rare:36 | ||||
| chr10:18659755-18659984 | Common:2; Rare:63 | ||||
| chr10:21524317-21524624 | Common:1; Rare:70 | ||||
| chr10:21525617-21525705 | Rare:17 | ||||
| chr10:23095344-23095627 | Rare:55 | ||||
| chr10:23344736-23344806 | Rare:26 | ||||
| chr10:24466292-24466560 | Rare:40 | ||||
| chr10:24722572-24722932 | Common:1; Rare:89 | ||||
| chr10:24952572-24952911 | Common:3; Rare:103 | ||||
| chr10:25016323-25016685 | Common:9; Rare:127 | ||||
| chr10:25016959-25017076 | Common:3; Rare:46 | ||||
| chr10:27100157-27100587 | Common:5; Rare:161; Clinvar:11; Clinvar (benign):5 | ||||
| chr10:27154161-27154535 | Rare:106 |