| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3797449-3797820 | Rare:134 | ||||
| chr11:3808448-3808608 | Common:1; Rare:48 | ||||
| chr11:3840915-3841085 | Rare:72 | ||||
| chr11:3855540-3855711 | Common:2; Rare:35 | ||||
| chr11:4094618-4094982 | Common:1; Rare:99 | ||||
| chr11:4393654-4393826 | Rare:41 | ||||
| chr11:4608140-4608405 | Common:1; Rare:78 | ||||
| chr11:5596610-5596736 | Common:3; Rare:46 | ||||
| chr11:5596738-5596751 | Rare:5 | ||||
| chr11:5624882-5625029 | Rare:25 | ||||
| chr11:6390214-6390503 | Common:2; Rare:83 | ||||
| chr11:6419058-6419176 | Common:2; Rare:25 | ||||
| chr11:6473884-6474067 | Rare:60 | ||||
| chr11:6481283-6481585 | Common:5; Rare:132 | ||||
| chr11:6603542-6603831 | Common:4; Rare:88; Clinvar (benign):3 |