| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67353473-67353830 | Common:2; Rare:90 | ||||
| chr11:67401774-67402075 | Common:3; Rare:113 | ||||
| chr11:67443458-67443591 | Common:1; Rare:46 | ||||
| chr11:67482923-67483192 | Rare:61; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67508038-67508109 | Rare:18 | ||||
| chr11:67508111-67508492 | Common:1; Rare:86 | ||||
| chr11:67508627-67508778 | Common:3; Rare:54 | ||||
| chr11:68038940-68039078 | Rare:44; Clinvar:1 | ||||
| chr11:68271891-68272010 | Rare:56 | ||||
| chr11:68903770-68903938 | Common:4; Rare:79; Clinvar (benign):6 | ||||
| chr11:69640794-69641250 | Common:1; Rare:98 | ||||
| chr11:69641270-69641508 | Rare:65 | ||||
| chr11:69675309-69675523 | Rare:59 | ||||
| chr11:70398455-70398596 | Common:1; Rare:46 | ||||
| chr11:71448347-71448693 | Common:4; Rare:91; Clinvar:3; Clinvar (benign):1 |