| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46700904-46701068 | Common:3; Rare:42 | ||||
| chr11:46846224-46846428 | Common:1; Rare:57 | ||||
| chr11:46936646-46936811 | Common:2; Rare:51 | ||||
| chr11:47176827-47177140 | Common:1; Rare:135 | ||||
| chr11:47186408-47186536 | Rare:35 | ||||
| chr11:47248769-47248941 | Rare:68 | ||||
| chr11:47269529-47269684 | Common:1; Rare:52 | ||||
| chr11:47269974-47270184 | Common:1; Rare:69 | ||||
| chr11:47426412-47426632 | Rare:54 | ||||
| chr11:47565490-47565632 | Common:3; Rare:28 | ||||
| chr11:47578944-47579094 | Rare:77; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47848322-47848649 | Common:3; Rare:113 | ||||
| chr11:57311454-57311724 | Common:1; Rare:69 | ||||
| chr11:57324877-57325164 | Common:1; Rare:95 | ||||
| chr11:57335751-57335953 | Common:4; Rare:49 |