| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65961411-65961827 | Common:2; Rare:300 | ||||
| chr11:65961999-65962232 | Common:8; Rare:147 | ||||
| chr11:66001255-66001879 | Common:8; Rare:151 | ||||
| chr11:66002041-66002851 | Common:13; Rare:614; Clinvar:24; Clinvar (benign):9 | ||||
| chr11:66051843-66052650 | Common:21; Rare:447 | ||||
| chr11:66058690-66059100 | Common:2; Rare:208 | ||||
| chr11:66069410-66069940 | Common:2; Rare:151 | ||||
| chr11:66070013-66070589 | Common:7; Rare:363; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:66070693-66071190 | Common:2; Rare:161; Clinvar (benign):2 | ||||
| chr11:66256940-66257380 | Common:2; Rare:68 | ||||
| chr11:66257494-66257861 | Common:3; Rare:272 | ||||
| chr11:66257870-66258240 | Common:5; Rare:128 | ||||
| chr11:66258320-66258586 | Rare:106 | ||||
| chr11:66261870-66262150 | Rare:88 | ||||
| chr11:66268322-66268939 | Common:11; Rare:346 |