| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:2138306-2138609 | Common:2; Rare:70 | ||||
| chr11:2302950-2303232 | Common:2; Rare:63 | ||||
| chr11:2378549-2378836 | Common:2; Rare:44 | ||||
| chr11:2884082-2884240 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:2902065-2902330 | Common:1; Rare:60 | ||||
| chr11:2929609-2929819 | Common:1; Rare:55 | ||||
| chr11:2992247-2992514 | Common:2; Rare:103 | ||||
| chr11:3057363-3057531 | Rare:62 | ||||
| chr11:3379089-3379343 | Common:4; Rare:68 | ||||
| chr11:3797566-3797959 | Rare:132 | ||||
| chr11:3840903-3841102 | Rare:83 | ||||
| chr11:3855531-3855754 | Common:2; Rare:47 | ||||
| chr11:4094594-4094877 | Common:2; Rare:78 | ||||
| chr11:4393651-4393820 | Rare:42 | ||||
| chr11:5624889-5625029 | Rare:23 |