| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:59810751-59810918 | Common:2; Rare:57 | ||||
| chr11:59866365-59866765 | Common:2; Rare:111; Clinvar (pathogenic):1 | ||||
| chr11:60701365-60701514 | Rare:37 | ||||
| chr11:60841916-60842146 | Common:2; Rare:82 | ||||
| chr11:60906493-60906883 | Rare:93 | ||||
| chr11:60913846-60914063 | Rare:30 | ||||
| chr11:60914101-60914262 | Rare:42 | ||||
| chr11:60924366-60924499 | Rare:40 | ||||
| chr11:61161074-61161510 | Rare:269 | ||||
| chr11:61161586-61161853 | Common:1; Rare:79 | ||||
| chr11:61333050-61333462 | Common:1; Rare:140 | ||||
| chr11:61361819-61362644 | Common:4; Rare:203; Clinvar:11; Clinvar (benign):1 | ||||
| chr11:61392065-61392318 | Common:3; Rare:39 | ||||
| chr11:61392484-61392682 | Common:2; Rare:62; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:61429390-61429573 | Common:2; Rare:61 |