| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66268340-66268674 | Common:3; Rare:96 | ||||
| chr11:66278110-66278465 | Common:1; Rare:112 | ||||
| chr11:66278508-66278539 | Rare:5 | ||||
| chr11:66282188-66282323 | Rare:46 | ||||
| chr11:66288970-66289443 | Common:2; Rare:125 | ||||
| chr11:66291774-66291933 | Rare:42 | ||||
| chr11:66345010-66345270 | Common:1; Rare:68 | ||||
| chr11:66347535-66347917 | Common:6; Rare:93; Clinvar (benign):2 | ||||
| chr11:66348086-66348116 | Rare:14 | ||||
| chr11:66420793-66421059 | Common:1; Rare:73 | ||||
| chr11:66466691-66467008 | Rare:98 | ||||
| chr11:66480212-66480455 | Common:3; Rare:65 | ||||
| chr11:66510516-66510712 | Common:2; Rare:89; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr11:66546208-66546302 | Common:2; Rare:22 | ||||
| chr11:66593032-66593209 | Common:1; Rare:63 |