| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1559129-1559339 | Common:2; Rare:93 | ||||
| chr11:1559430-1559810 | Common:5; Rare:126 | ||||
| chr11:1572229-1572542 | Common:4; Rare:171 | ||||
| chr11:1763796-1764122 | Common:6; Rare:260; Clinvar:18; Clinvar (benign):16 | ||||
| chr11:2400249-2400817 | Common:11; Rare:293 | ||||
| chr11:2777336-2777572 | Common:2; Rare:42 | ||||
| chr11:2884010-2884670 | Common:2; Rare:243; Clinvar:5; Clinvar (benign):9 | ||||
| chr11:2902050-2902394 | Common:1; Rare:112 | ||||
| chr11:2928994-2929187 | Common:2; Rare:119 | ||||
| chr11:2929246-2929809 | Common:3; Rare:298 | ||||
| chr11:2991887-2992136 | Common:2; Rare:85 | ||||
| chr11:2992223-2992610 | Common:5; Rare:284 | ||||
| chr11:3057349-3057584 | Rare:177 | ||||
| chr11:3126547-3126747 | Common:2; Rare:91 | ||||
| chr11:3165237-3165363 | Common:1; Rare:40 |