| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66745142-66745277 | Rare:30 | ||||
| chr11:66745356-66745505 | Common:1; Rare:27 | ||||
| chr11:66842940-66843113 | Common:1; Rare:70 | ||||
| chr11:66843223-66843530 | Common:6; Rare:159 | ||||
| chr11:66843597-66843751 | Common:1; Rare:64 | ||||
| chr11:66843798-66843844 | Rare:15 | ||||
| chr11:66856098-66856627 | Common:1; Rare:167 | ||||
| chr11:66856769-66857130 | Common:1; Rare:102 | ||||
| chr11:66857485-66857649 | Rare:27 | ||||
| chr11:66958104-66958238 | Common:2; Rare:46 | ||||
| chr11:66958279-66958881 | Common:6; Rare:169; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:67006643-67006827 | Common:2; Rare:52 | ||||
| chr11:67056332-67056380 | Rare:4 | ||||
| chr11:67056652-67056931 | Common:1; Rare:76 | ||||
| chr11:67057195-67057273 | Rare:17 |