| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:8911008-8911333 | Common:8; Rare:173 | ||||
| chr11:8963975-8964310 | Common:2; Rare:168 | ||||
| chr11:8964384-8964628 | Common:7; Rare:126 | ||||
| chr11:8964630-8964840 | Rare:95 | ||||
| chr11:8964849-8964992 | Common:2; Rare:34 | ||||
| chr11:9265261-9265452 | Rare:108 | ||||
| chr11:9314453-9314888 | Common:10; Rare:271 | ||||
| chr11:9384512-9384800 | Common:2; Rare:203 | ||||
| chr11:9384980-9385660 | Common:4; Rare:258 | ||||
| chr11:9460580-9461048 | Common:8; Rare:232 | ||||
| chr11:9573358-9573827 | Common:4; Rare:246 | ||||
| chr11:9573992-9574412 | Common:7; Rare:165 | ||||
| chr11:9663984-9664195 | Common:8; Rare:140 | ||||
| chr11:10293909-10294051 | Common:3; Rare:35; Clinvar (pathogenic):1 | ||||
| chr11:10294005-10294132 | Rare:28; Clinvar:1; Clinvar (pathogenic):1 |