| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67469219-67469380 | Common:1; Rare:48 | ||||
| chr11:67482901-67483154 | Rare:57; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:67505177-67505446 | Rare:66 | ||||
| chr11:67508156-67508454 | Common:1; Rare:57 | ||||
| chr11:67508627-67508797 | Common:3; Rare:66 | ||||
| chr11:68030302-68030733 | Common:3; Rare:124; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68121409-68121624 | Common:1; Rare:59 | ||||
| chr11:68213480-68213993 | Common:1; Rare:293 | ||||
| chr11:68271899-68272139 | Common:2; Rare:100 | ||||
| chr11:68460210-68460370 | Common:2; Rare:67 | ||||
| chr11:68460560-68460809 | Common:3; Rare:86 | ||||
| chr11:68903748-68903943 | Common:4; Rare:87; Clinvar (benign):6 | ||||
| chr11:69048728-69049000 | Common:6; Rare:100 | ||||
| chr11:69675281-69675501 | Rare:65 | ||||
| chr11:70203133-70203366 | Common:3; Rare:87 |