| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47402968-47403206 | Common:1; Rare:112; Clinvar:38; Clinvar (benign):29; Clinvar (pathogenic):1 | ||||
| chr2:47782956-47783189 | Common:2; Rare:103; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:47905496-47905828 | Common:3; Rare:162 | ||||
| chr2:48314161-48314802 | Common:1; Rare:223 | ||||
| chr2:48314837-48315073 | Common:1; Rare:104 | ||||
| chr2:48440614-48440900 | Common:8; Rare:125 | ||||
| chr2:53767559-53767949 | Common:5; Rare:147 | ||||
| chr2:53786815-53787229 | Common:1; Rare:155 | ||||
| chr2:53970788-53971157 | Common:11; Rare:134 | ||||
| chr2:54115843-54115993 | Common:3; Rare:54 | ||||
| chr2:54456123-54456447 | Rare:120 | ||||
| chr2:54457066-54457268 | Common:1; Rare:85 | ||||
| chr2:55049116-55049156 | Rare:7 | ||||
| chr2:55050327-55050382 | Rare:21 | ||||
| chr2:55050441-55050952 | Common:8; Rare:156 |