| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65635033-65635236 | Rare:68 | ||||
| chr11:65790923-65790967 | Rare:9 | ||||
| chr11:65791388-65791403 | Rare:5 | ||||
| chr11:65792227-65792415 | Rare:28 | ||||
| chr11:65899208-65899415 | Common:1; Rare:47 | ||||
| chr11:66682859-66682902 | Rare:6 | ||||
| chr11:66682994-66683137 | Common:2; Rare:20 | ||||
| chr11:66683386-66683779 | Common:3; Rare:78 | ||||
| chr11:66683783-66684143 | Common:5; Rare:56 | ||||
| chr11:66705367-66705682 | Rare:102; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:66708293-66708309 | Rare:5 | ||||
| chr11:66711141-66711198 | Rare:5 | ||||
| chr11:66717567-66717768 | Rare:31 | ||||
| chr11:66718469-66718966 | Common:4; Rare:121 | ||||
| chr11:66725658-66725735 | Rare:16 |