| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47176440-47176877 | Common:4; Rare:196; Clinvar (benign):5 | ||||
| chr2:47402943-47403172 | Common:1; Rare:101; Clinvar:32; Clinvar (benign):21 | ||||
| chr2:47905489-47905835 | Common:3; Rare:168 | ||||
| chr2:48440631-48440884 | Common:7; Rare:119 | ||||
| chr2:48529242-48529399 | Common:1; Rare:42 | ||||
| chr2:53767559-53767866 | Common:4; Rare:106 | ||||
| chr2:53786842-53787191 | Common:1; Rare:135 | ||||
| chr2:53970725-53971152 | Common:11; Rare:163 | ||||
| chr2:54115469-54115678 | Rare:69 | ||||
| chr2:54457096-54457274 | Common:1; Rare:77 | ||||
| chr2:55050190-55050436 | Common:1; Rare:82 | ||||
| chr2:55050441-55050754 | Common:4; Rare:95 | ||||
| chr2:55232249-55232725 | Common:3; Rare:133 | ||||
| chr2:55519411-55519870 | Common:2; Rare:152 | ||||
| chr2:58046604-58046845 | Rare:73 |