| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:59172124-59172190 | Common:1; Rare:18 | ||||
| chr11:59212872-59212983 | Rare:37 | ||||
| chr11:59668980-59669328 | Rare:121 | ||||
| chr11:59754949-59755120 | Rare:32 | ||||
| chr11:59755284-59755553 | Common:2; Rare:81 | ||||
| chr11:59841020-59841379 | Common:1; Rare:95 | ||||
| chr11:59845332-59845848 | Common:1; Rare:106; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:59866466-59866661 | Common:1; Rare:31 | ||||
| chr11:60182495-60182587 | Rare:13 | ||||
| chr11:60183721-60184063 | Common:1; Rare:72 | ||||
| chr11:60699422-60699754 | Common:3; Rare:58 | ||||
| chr11:60841916-60842146 | Common:2; Rare:82 | ||||
| chr11:60847762-60847971 | Common:1; Rare:53 | ||||
| chr11:60906399-60906787 | Rare:101 | ||||
| chr11:60913981-60914257 | Common:1; Rare:67 |