| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9314623-9314920 | Common:3; Rare:80 | ||||
| chr11:9460697-9461030 | Common:3; Rare:92 | ||||
| chr11:10541144-10541293 | Rare:53 | ||||
| chr11:10751188-10751279 | Rare:28 | ||||
| chr11:10858023-10858236 | Common:2; Rare:61 | ||||
| chr11:13463168-13463366 | Common:1; Rare:75 | ||||
| chr11:14643631-14643680 | Rare:20 | ||||
| chr11:16738466-16738690 | Common:2; Rare:46 | ||||
| chr11:17014255-17014330 | Rare:28 | ||||
| chr11:17207910-17208111 | Common:2; Rare:76 | ||||
| chr11:18322131-18322332 | Common:5; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322457-18322607 | Common:2; Rare:62 | ||||
| chr11:18526847-18526972 | Rare:62 | ||||
| chr11:18634330-18634580 | Common:2; Rare:79 | ||||
| chr11:20363659-20363753 | Common:1; Rare:21 |