| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38751354-38751646 | Common:4; Rare:130 | ||||
| chr2:38875902-38876047 | Common:1; Rare:49 | ||||
| chr2:39437115-39437456 | Common:4; Rare:121 | ||||
| chr2:42169151-42169399 | Common:1; Rare:128 | ||||
| chr2:43595992-43596209 | Common:1; Rare:74 | ||||
| chr2:46617037-46617252 | Common:6; Rare:80 | ||||
| chr2:46915733-46915908 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47402947-47403183 | Common:1; Rare:107; Clinvar:32; Clinvar (benign):24 | ||||
| chr2:47782956-47783161 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:53786862-53787181 | Common:1; Rare:118 | ||||
| chr2:53970788-53971095 | Common:9; Rare:97 | ||||
| chr2:54558664-54558772 | Common:1; Rare:29 | ||||
| chr2:55232316-55232726 | Common:2; Rare:117 | ||||
| chr2:55269163-55269411 | Common:3; Rare:67 | ||||
| chr2:58241311-58241398 | Rare:57; Clinvar:3; Clinvar (benign):1 |