| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74311580-74311789 | Common:1; Rare:71 | ||||
| chr11:74398333-74398609 | Common:9; Rare:156 | ||||
| chr11:74398670-74399024 | Rare:183 | ||||
| chr11:74493023-74493480 | Common:3; Rare:417; Clinvar (pathogenic):3 | ||||
| chr11:74493583-74493847 | Common:3; Rare:235; Clinvar (pathogenic):1 | ||||
| chr11:74592457-74592686 | Common:3; Rare:192 | ||||
| chr11:74748648-74748979 | Common:4; Rare:140 | ||||
| chr11:74749160-74749680 | Common:7; Rare:204 | ||||
| chr11:74948999-74949379 | Common:20; Rare:299 | ||||
| chr11:74988634-74989091 | Rare:167 | ||||
| chr11:75351520-75351941 | Common:7; Rare:233 | ||||
| chr11:75399366-75399646 | Common:5; Rare:114 | ||||
| chr11:75399992-75400184 | Common:1; Rare:37 | ||||
| chr11:75430098-75430405 | Common:3; Rare:322 | ||||
| chr11:75430418-75430539 | Rare:50 |