| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:19240507-19240556 | Rare:11 | ||||
| chr11:19240596-19240707 | Rare:22 | ||||
| chr11:19240825-19241437 | Common:1; Rare:171 | ||||
| chr11:19241597-19241997 | Common:2; Rare:107 | ||||
| chr11:19712608-19712879 | Common:2; Rare:106 | ||||
| chr11:19777461-19777833 | Common:2; Rare:94 | ||||
| chr11:19777986-19778041 | Rare:11 | ||||
| chr11:20363614-20363848 | Common:4; Rare:46 | ||||
| chr11:20363972-20364136 | Common:7; Rare:32 | ||||
| chr11:20387160-20387785 | Common:10; Rare:182 | ||||
| chr11:22192814-22193158 | Rare:82 | ||||
| chr11:22193257-22193410 | Common:7; Rare:24; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:22193666-22193846 | Common:1; Rare:46 | ||||
| chr11:22625120-22625319 | Common:2; Rare:83; Clinvar:6; Clinvar (benign):5 | ||||
| chr11:22625414-22625641 | Common:3; Rare:108; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):2 |