| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46700551-46701094 | Common:4; Rare:143 | ||||
| chr11:46846207-46846443 | Common:1; Rare:68 | ||||
| chr11:47167898-47168198 | Common:1; Rare:86 | ||||
| chr11:47176833-47177194 | Common:1; Rare:150 | ||||
| chr11:47237853-47238183 | Common:1; Rare:82; Clinvar:2 | ||||
| chr11:47248783-47248964 | Rare:74 | ||||
| chr11:47257794-47257994 | Rare:42 | ||||
| chr11:47426205-47426271 | Rare:28 | ||||
| chr11:47553051-47553373 | Common:2; Rare:113 | ||||
| chr11:47565490-47565780 | Common:4; Rare:69 | ||||
| chr11:47578932-47579327 | Rare:189; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:47638708-47639051 | Common:5; Rare:90 | ||||
| chr11:47727394-47727411 | Rare:2 | ||||
| chr11:47767092-47767411 | Common:6; Rare:137 | ||||
| chr11:47848281-47848640 | Common:4; Rare:134 |