| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1933791-1934000 | Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:2138503-2138583 | Common:1; Rare:14 | ||||
| chr11:2138626-2138735 | Rare:23 | ||||
| chr11:2138838-2138888 | Rare:9 | ||||
| chr11:2138891-2139068 | Common:1; Rare:31 | ||||
| chr11:2140899-2140960 | Rare:14 | ||||
| chr11:2140965-2141032 | Rare:10 | ||||
| chr11:2884100-2884252 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:2902065-2902291 | Common:1; Rare:48 | ||||
| chr11:3797474-3797815 | Rare:125 | ||||
| chr11:3840916-3841090 | Rare:72 | ||||
| chr11:4094749-4094897 | Rare:45 | ||||
| chr11:4393665-4393803 | Rare:32 | ||||
| chr11:5624894-5625057 | Rare:27 | ||||
| chr11:6234621-6234786 | Common:2; Rare:52 |