| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:747329-747499 | Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:777459-777598 | Common:1; Rare:61 | ||||
| chr11:809525-809582 | Rare:14 | ||||
| chr11:821829-821994 | Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:832833-833022 | Common:7; Rare:64 | ||||
| chr11:842416-842980 | Common:8; Rare:231 | ||||
| chr11:843934-844159 | Common:1; Rare:58 | ||||
| chr11:1309538-1309851 | Common:3; Rare:132 | ||||
| chr11:2301866-2302136 | Common:2; Rare:70 | ||||
| chr11:2302908-2303189 | Common:1; Rare:74 | ||||
| chr11:2461310-2461470 | Common:1; Rare:48 | ||||
| chr11:3379096-3379318 | Common:3; Rare:57 | ||||
| chr11:3641989-3642212 | Common:9; Rare:79 | ||||
| chr11:3797500-3797840 | Rare:119 | ||||
| chr11:3855551-3855735 | Common:2; Rare:36 |