| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32165737-32165895 | Common:1; Rare:58 | ||||
| chr2:37084328-37084536 | Common:3; Rare:75 | ||||
| chr2:37231550-37231651 | Common:1; Rare:52 | ||||
| chr2:37324713-37324896 | Common:1; Rare:76 | ||||
| chr2:38076143-38076278 | Rare:34 | ||||
| chr2:38751354-38751532 | Common:2; Rare:77 | ||||
| chr2:38875880-38876036 | Common:2; Rare:53 | ||||
| chr2:39437116-39437463 | Common:4; Rare:121 | ||||
| chr2:39779215-39779298 | Common:2; Rare:32 | ||||
| chr2:43226597-43226862 | Common:2; Rare:103 | ||||
| chr2:43899317-43899501 | Rare:54 | ||||
| chr2:46616974-46617252 | Common:6; Rare:111 | ||||
| chr2:46915723-46915878 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:48440621-48440824 | Common:6; Rare:89 | ||||
| chr2:53786852-53787206 | Common:1; Rare:135 |