| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43358793-43359295 | Rare:269 | ||||
| chr11:43644040-43644270 | Common:1; Rare:63 | ||||
| chr11:44065970-44066530 | Common:8; Rare:226 | ||||
| chr11:44565140-44565687 | Common:7; Rare:199 | ||||
| chr11:45146316-45146481 | Common:1; Rare:28 | ||||
| chr11:45147080-45147450 | Common:2; Rare:242 | ||||
| chr11:45804258-45804471 | Common:2; Rare:78 | ||||
| chr11:45804810-45805300 | Common:6; Rare:173; Clinvar:11; Clinvar (benign):2 | ||||
| chr11:45847249-45847492 | Common:4; Rare:189 | ||||
| chr11:45917715-45918190 | Common:1; Rare:171; Clinvar:6; Clinvar (benign):1 | ||||
| chr11:45918773-45918907 | Rare:41 | ||||
| chr11:46119110-46119740 | Common:5; Rare:199 | ||||
| chr11:46119683-46120083 | Common:12; Rare:202 | ||||
| chr11:46120889-46121350 | Common:4; Rare:109 | ||||
| chr11:46121354-46121607 | Rare:115 |