| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67464574-67465018 | Rare:208 | ||||
| chr11:67469118-67469478 | Common:4; Rare:125 | ||||
| chr11:67482670-67483199 | Common:2; Rare:119; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr11:67483207-67483399 | Rare:71; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr11:67505286-67505510 | Rare:53 | ||||
| chr11:67507820-67507897 | Rare:15 | ||||
| chr11:67508019-67508538 | Common:1; Rare:124 | ||||
| chr11:67508582-67508835 | Common:3; Rare:88 | ||||
| chr11:67583486-67583501 | Rare:5 | ||||
| chr11:67583527-67583933 | Common:3; Rare:115 | ||||
| chr11:67584259-67584506 | Common:2; Rare:66 | ||||
| chr11:67606718-67607064 | Common:1; Rare:116; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:67629320-67629541 | Common:1; Rare:49 | ||||
| chr11:67629859-67630014 | Rare:36 | ||||
| chr11:67630172-67630562 | Common:6; Rare:69 |