| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:117200581-117200824 | Common:3; Rare:58 | ||||
| chr11:117201093-117201424 | Common:3; Rare:62 | ||||
| chr11:117202071-117202267 | Common:3; Rare:44 | ||||
| chr11:117218540-117218698 | Rare:26 | ||||
| chr11:117218811-117218872 | Rare:10 | ||||
| chr11:117219085-117219342 | Common:1; Rare:54 | ||||
| chr11:117232025-117232168 | Rare:36 | ||||
| chr11:117232493-117232758 | Common:2; Rare:85 | ||||
| chr11:117316250-117316413 | Common:1; Rare:35 | ||||
| chr11:117876593-117876836 | Rare:65 | ||||
| chr11:117986260-117986473 | Common:4; Rare:81; Clinvar:2 | ||||
| chr11:118264252-118264643 | Common:1; Rare:57 | ||||
| chr11:118344268-118344421 | Common:1; Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:118401320-118401746 | Common:1; Rare:139 | ||||
| chr11:118531105-118531298 | Rare:65 |