| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3057346-3057553 | Rare:140 | ||||
| chr11:3379060-3379440 | Common:8; Rare:154 | ||||
| chr11:3797432-3797944 | Rare:373 | ||||
| chr11:3808504-3808634 | Common:2; Rare:44 | ||||
| chr11:3840883-3841180 | Common:2; Rare:196 | ||||
| chr11:3855027-3855219 | Common:2; Rare:49 | ||||
| chr11:3855551-3855788 | Common:4; Rare:78 | ||||
| chr11:3855800-3856360 | Common:2; Rare:206; Clinvar:1 | ||||
| chr11:4094558-4094909 | Common:4; Rare:183 | ||||
| chr11:5624840-5625020 | Rare:28 | ||||
| chr11:6390174-6390512 | Common:4; Rare:164 | ||||
| chr11:6473855-6474088 | Rare:79 | ||||
| chr11:6481284-6481647 | Common:10; Rare:284 | ||||
| chr11:6603519-6603880 | Common:8; Rare:202; Clinvar (benign):6 | ||||
| chr11:6612157-6612331 | Common:4; Rare:125 |