| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10541159-10541323 | Rare:58 | ||||
| chr11:10751087-10751297 | Rare:65 | ||||
| chr11:10808877-10809117 | Common:1; Rare:102 | ||||
| chr11:10858013-10858269 | Common:3; Rare:83 | ||||
| chr11:11621989-11622212 | Common:2; Rare:85 | ||||
| chr11:11841903-11842066 | Common:1; Rare:48 | ||||
| chr11:12377472-12377630 | Rare:61 | ||||
| chr11:13463159-13463395 | Common:1; Rare:88 | ||||
| chr11:14520318-14520545 | Rare:74 | ||||
| chr11:14643631-14643810 | Common:1; Rare:68 | ||||
| chr11:14891637-14891770 | Rare:35 | ||||
| chr11:16738453-16738717 | Common:3; Rare:58 | ||||
| chr11:17207920-17208111 | Common:1; Rare:72 | ||||
| chr11:17276621-17276827 | Common:3; Rare:53; Clinvar:3 | ||||
| chr11:18322086-18322285 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):2 |