| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43595967-43596143 | Common:1; Rare:55 | ||||
| chr2:43899316-43899535 | Rare:67; Clinvar:1 | ||||
| chr2:44361398-44361990 | Common:3; Rare:194 | ||||
| chr2:45651555-45651685 | Common:1; Rare:36 | ||||
| chr2:46616974-46617270 | Common:7; Rare:131 | ||||
| chr2:46915718-46916166 | Common:4; Rare:150; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46941715-46941844 | Common:2; Rare:42; Clinvar (benign):1 | ||||
| chr2:47402915-47403197 | Common:1; Rare:129; Clinvar:43; Clinvar (benign):27 | ||||
| chr2:47905493-47905570 | Common:1; Rare:37 | ||||
| chr2:53786839-53787305 | Common:1; Rare:183 | ||||
| chr2:53970991-53971122 | Common:4; Rare:51 | ||||
| chr2:54973560-54973875 | Common:3; Rare:96 | ||||
| chr2:55050137-55050382 | Rare:97 | ||||
| chr2:55050385-55050748 | Common:5; Rare:108 | ||||
| chr2:55232246-55232730 | Common:3; Rare:136 |