| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66345027-66345262 | Common:1; Rare:64 | ||||
| chr11:66347613-66347933 | Common:6; Rare:73 | ||||
| chr11:66347988-66348118 | Rare:44 | ||||
| chr11:66371050-66371510 | Rare:127 | ||||
| chr11:66371723-66372069 | Common:1; Rare:87 | ||||
| chr11:66372078-66372215 | Common:2; Rare:29 | ||||
| chr11:66438747-66439254 | Common:2; Rare:117 | ||||
| chr11:66466679-66466848 | Rare:40 | ||||
| chr11:66479925-66480059 | Rare:25 | ||||
| chr11:66480171-66480464 | Common:3; Rare:86 | ||||
| chr11:66480645-66480754 | Common:1; Rare:34 | ||||
| chr11:66510524-66510694 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:66545990-66546194 | Common:3; Rare:52 | ||||
| chr11:66593013-66593232 | Common:1; Rare:78 | ||||
| chr11:66616153-66616668 | Common:1; Rare:151 |