| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57476432-57476602 | Rare:42 | ||||
| chr11:57547235-57547441 | Common:1; Rare:30 | ||||
| chr11:57547971-57548220 | Common:2; Rare:48 | ||||
| chr11:57566258-57566393 | Rare:14 | ||||
| chr11:57788544-57788603 | Rare:10 | ||||
| chr11:57792313-57792505 | Common:1; Rare:54 | ||||
| chr11:58573545-58573615 | Rare:12 | ||||
| chr11:58573616-58574035 | Rare:86 | ||||
| chr11:58647228-58647428 | Common:1; Rare:41 | ||||
| chr11:59098039-59098193 | Common:1; Rare:30 | ||||
| chr11:59102307-59102399 | Common:3; Rare:22 | ||||
| chr11:59106014-59106347 | Common:1; Rare:68 | ||||
| chr11:59151801-59152012 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr11:59173977-59174012 | Rare:11 | ||||
| chr11:59284644-59284770 | Rare:26 |