| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:30422517-30422831 | Common:2; Rare:47 | ||||
| chr11:30480262-30480475 | Common:1; Rare:43 | ||||
| chr11:30585488-30585562 | Rare:22 | ||||
| chr11:30749202-30749375 | Rare:35 | ||||
| chr11:30789351-30789480 | Rare:18 | ||||
| chr11:31150921-31151053 | Common:1; Rare:17 | ||||
| chr11:31508802-31509041 | Rare:39 | ||||
| chr11:31813573-31813677 | Common:1; Rare:20 | ||||
| chr11:31813982-31814044 | Rare:7 | ||||
| chr11:31815174-31815343 | Rare:33 | ||||
| chr11:31815783-31815870 | Common:1; Rare:13 | ||||
| chr11:32333257-32333459 | Common:2; Rare:41 | ||||
| chr11:32386831-32387018 | Common:1; Rare:34 | ||||
| chr11:32392166-32392718 | Rare:79; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:32438063-32438091 | Rare:15 |