| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3057369-3057538 | Rare:59 | ||||
| chr11:3379073-3379290 | Common:3; Rare:59 | ||||
| chr11:3840910-3841102 | Rare:79 | ||||
| chr11:4094592-4094701 | Common:1; Rare:29 | ||||
| chr11:4094716-4094877 | Common:1; Rare:45 | ||||
| chr11:4393658-4393803 | Rare:34 | ||||
| chr11:4608192-4608416 | Common:1; Rare:61 | ||||
| chr11:5624894-5625023 | Rare:17 | ||||
| chr11:6234621-6234755 | Common:2; Rare:43 | ||||
| chr11:6390311-6390474 | Common:1; Rare:44 | ||||
| chr11:6419028-6419385 | Common:4; Rare:89 | ||||
| chr11:6473855-6474102 | Rare:81 | ||||
| chr11:6481292-6481542 | Common:4; Rare:109 | ||||
| chr11:6603542-6603815 | Common:4; Rare:83; Clinvar (benign):3 | ||||
| chr11:6619409-6619559 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):5 |