| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:209423970-209424260 | Common:3; Rare:81 | ||||
| chr2:209579227-209579365 | Common:8; Rare:23 | ||||
| chr2:209579390-209579744 | Common:1; Rare:62 | ||||
| chr2:209661331-209661579 | Common:2; Rare:41 | ||||
| chr2:210002473-210002660 | Common:5; Rare:61 | ||||
| chr2:212538569-212538892 | Common:1; Rare:99 | ||||
| chr2:212539055-212539342 | Common:7; Rare:56 | ||||
| chr2:213284238-213284509 | Rare:91 | ||||
| chr2:214410814-214411211 | Common:3; Rare:70 | ||||
| chr2:215311969-215312115 | Common:5; Rare:64 | ||||
| chr2:215372329-215372433 | Rare:32 | ||||
| chr2:215436006-215436234 | Common:2; Rare:72 | ||||
| chr2:216081756-216081932 | Common:1; Rare:62 | ||||
| chr2:216412260-216412538 | Common:2; Rare:63; Clinvar (benign):1 | ||||
| chr2:216412688-216412782 | Rare:10 |