| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:86521749-86521960 | Rare:69 | ||||
| chr10:87094996-87095206 | Common:1; Rare:42 | ||||
| chr10:87504808-87504931 | Common:1; Rare:56 | ||||
| chr10:87818135-87818366 | Common:2; Rare:79 | ||||
| chr10:89327773-89327996 | Common:3; Rare:37 | ||||
| chr10:89414675-89414785 | Common:3; Rare:53 | ||||
| chr10:89701391-89701652 | Common:2; Rare:83 | ||||
| chr10:91410240-91410494 | Common:2; Rare:94 | ||||
| chr10:91923716-91923841 | Common:1; Rare:52 | ||||
| chr10:92574049-92574104 | Common:1; Rare:16 | ||||
| chr10:92592972-92593169 | Common:3; Rare:60 | ||||
| chr10:92848368-92848528 | Rare:57 | ||||
| chr10:93496413-93496647 | Common:3; Rare:60 | ||||
| chr10:93702497-93702699 | Common:4; Rare:74 | ||||
| chr10:93757684-93758043 | Common:1; Rare:61; Clinvar:3; Clinvar (benign):1 |