| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:54557436-54558071 | Common:4; Rare:225 | ||||
| chr2:54558278-54558841 | Common:10; Rare:316 | ||||
| chr2:54723320-54723810 | Common:4; Rare:287 | ||||
| chr2:55048820-55049894 | Common:3; Rare:406 | ||||
| chr2:55050137-55050802 | Common:9; Rare:325 | ||||
| chr2:55232096-55232729 | Common:10; Rare:332 | ||||
| chr2:55269129-55269338 | Common:4; Rare:108 | ||||
| chr2:55419773-55420173 | Common:9; Rare:290 | ||||
| chr2:55519415-55519777 | Common:2; Rare:206 | ||||
| chr2:55618790-55619030 | Common:2; Rare:106 | ||||
| chr2:55693805-55693993 | Common:1; Rare:60; Clinvar (benign):2 | ||||
| chr2:58046601-58046887 | Common:4; Rare:169 | ||||
| chr2:58047060-58047390 | Rare:165 | ||||
| chr2:58241309-58241425 | Rare:116; Clinvar:7; Clinvar (benign):2 | ||||
| chr2:60881335-60881697 | Common:5; Rare:236 |