| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73377163-73377399 | Rare:44 | ||||
| chr11:73597963-73598847 | Common:16; Rare:213 | ||||
| chr11:73760905-73761425 | Common:5; Rare:139 | ||||
| chr11:73787752-73788304 | Common:8; Rare:147 | ||||
| chr11:73876487-73877067 | Common:5; Rare:157 | ||||
| chr11:73980369-73980443 | Rare:12 | ||||
| chr11:73981090-73981188 | Rare:24 | ||||
| chr11:73981296-73981445 | Common:1; Rare:19 | ||||
| chr11:73982666-73983077 | Common:8; Rare:117 | ||||
| chr11:73983140-73983612 | Common:4; Rare:105 | ||||
| chr11:74170819-74171439 | Common:4; Rare:196 | ||||
| chr11:74398365-74398589 | Common:3; Rare:61 | ||||
| chr11:74398669-74399137 | Common:1; Rare:136 | ||||
| chr11:74493070-74493458 | Common:1; Rare:148; Clinvar (pathogenic):1 | ||||
| chr11:74493631-74493784 | Common:1; Rare:60 |