| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:21123833-21123992 | Common:1; Rare:52 | ||||
| chr2:23927067-23927295 | Common:3; Rare:82 | ||||
| chr2:23940366-23940538 | Common:3; Rare:62 | ||||
| chr2:24076226-24076590 | Rare:100 | ||||
| chr2:24123272-24123512 | Common:1; Rare:64 | ||||
| chr2:24971907-24972143 | Common:1; Rare:75 | ||||
| chr2:26033803-26034151 | Common:3; Rare:118 | ||||
| chr2:26244573-26244972 | Common:2; Rare:147; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345798-26346152 | Common:1; Rare:103 | ||||
| chr2:26764210-26764312 | Rare:36 | ||||
| chr2:27032862-27033009 | Rare:57 | ||||
| chr2:27071551-27071884 | Common:1; Rare:100 | ||||
| chr2:27078516-27078778 | Common:2; Rare:67 | ||||
| chr2:27211920-27212065 | Common:3; Rare:59 | ||||
| chr2:27212225-27212366 | Common:1; Rare:76 |