| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45590587-45590801 | Common:5; Rare:70 | ||||
| chr21:45590956-45591028 | Common:1; Rare:20 | ||||
| chr21:45612180-45612291 | Common:1; Rare:25 | ||||
| chr21:46667331-46667428 | Common:3; Rare:36 | ||||
| chr22:19171572-19171731 | Rare:61 | ||||
| chr22:19176652-19176864 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:19455481-19455695 | Common:1; Rare:35 | ||||
| chr22:20206286-20206397 | Common:2; Rare:27 | ||||
| chr22:21014156-21014386 | Rare:59 | ||||
| chr22:21045041-21045290 | Common:3; Rare:44 | ||||
| chr22:22298029-22298238 | Common:6; Rare:92 | ||||
| chr22:22306810-22307018 | Common:3; Rare:52 | ||||
| chr22:23913915-23914219 | Common:3; Rare:122 | ||||
| chr22:25447963-25448178 | Common:4; Rare:77 | ||||
| chr22:26672632-26672786 | Common:2; Rare:39 |