| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74398290-74398650 | Common:6; Rare:166 | ||||
| chr11:74462110-74462318 | Common:4; Rare:51 | ||||
| chr11:74493010-74493400 | Common:2; Rare:249; Clinvar (pathogenic):2 | ||||
| chr11:74493660-74493816 | Common:2; Rare:106 | ||||
| chr11:74748615-74748902 | Common:6; Rare:125 | ||||
| chr11:74948946-74949372 | Common:15; Rare:232 | ||||
| chr11:74988785-74989017 | Rare:62 | ||||
| chr11:75159563-75159869 | Common:2; Rare:88 | ||||
| chr11:75351583-75351905 | Common:6; Rare:173 | ||||
| chr11:75525806-75526065 | Common:4; Rare:142 | ||||
| chr11:75561956-75562480 | Common:2; Rare:177; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:75562540-75562930 | Common:2; Rare:144 | ||||
| chr11:75563155-75563560 | Rare:133 | ||||
| chr11:75719782-75720009 | Common:3; Rare:123 | ||||
| chr11:75768439-75768879 | Common:9; Rare:257 |