| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46699076-46699438 | Common:2; Rare:106 | ||||
| chr2:46915723-46915895 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46915975-46916166 | Common:2; Rare:61 | ||||
| chr2:46941707-46941844 | Common:2; Rare:46; Clinvar (benign):1 | ||||
| chr2:47905492-47905621 | Common:2; Rare:69 | ||||
| chr2:48440621-48440847 | Common:8; Rare:107 | ||||
| chr2:53786839-53787253 | Common:1; Rare:161 | ||||
| chr2:53970782-53971126 | Common:10; Rare:116 | ||||
| chr2:54973560-54973867 | Common:3; Rare:96 | ||||
| chr2:55050140-55050748 | Common:5; Rare:203 | ||||
| chr2:55232246-55232726 | Common:3; Rare:136 | ||||
| chr2:58046750-58046872 | Common:2; Rare:43 | ||||
| chr2:61017178-61017760 | Common:4; Rare:168; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61144926-61145187 | Common:3; Rare:84 | ||||
| chr2:61471159-61471378 | Common:2; Rare:84 |