| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46617019-46617255 | Common:6; Rare:99 | ||||
| chr2:46915722-46915895 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176440-47176871 | Common:4; Rare:194; Clinvar (benign):5 | ||||
| chr2:48440631-48440921 | Common:7; Rare:127 | ||||
| chr2:53767559-53767871 | Common:5; Rare:109 | ||||
| chr2:53786862-53787090 | Rare:78 | ||||
| chr2:53970788-53971152 | Common:11; Rare:131 | ||||
| chr2:55050272-55050408 | Common:1; Rare:55 | ||||
| chr2:55050417-55050763 | Common:4; Rare:103 | ||||
| chr2:55232242-55232726 | Common:3; Rare:136 | ||||
| chr2:55519414-55519765 | Common:1; Rare:99 | ||||
| chr2:58046733-58046845 | Rare:36 | ||||
| chr2:61017425-61017771 | Common:1; Rare:109; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:61144921-61145184 | Common:3; Rare:86 | ||||
| chr2:61177268-61177487 | Common:5; Rare:96 |