| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10808877-10809119 | Common:1; Rare:105 | ||||
| chr11:10858023-10858260 | Common:2; Rare:76 | ||||
| chr11:11621984-11622281 | Common:4; Rare:109 | ||||
| chr11:11841938-11842077 | Common:1; Rare:39 | ||||
| chr11:12473816-12473980 | Rare:51 | ||||
| chr11:13009127-13009323 | Common:1; Rare:71 | ||||
| chr11:13463090-13463403 | Common:1; Rare:112 | ||||
| chr11:14520306-14520532 | Rare:75 | ||||
| chr11:14643631-14643758 | Common:1; Rare:58 | ||||
| chr11:14891641-14891893 | Rare:57 | ||||
| chr11:16738466-16738839 | Common:3; Rare:88 | ||||
| chr11:17013849-17013979 | Common:6; Rare:55 | ||||
| chr11:17077618-17077836 | Common:2; Rare:89 | ||||
| chr11:17207905-17208111 | Common:2; Rare:80 | ||||
| chr11:18322131-18322626 | Common:8; Rare:175; Clinvar:1; Clinvar (benign):2 |