| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74749246-74749364 | Rare:32 | ||||
| chr11:74948643-74948685 | Rare:5 | ||||
| chr11:74948951-74949438 | Common:8; Rare:151 | ||||
| chr11:74988628-74988761 | Rare:27 | ||||
| chr11:74988784-74989024 | Rare:64 | ||||
| chr11:75241135-75241388 | Rare:69 | ||||
| chr11:75312155-75312271 | Common:2; Rare:22 | ||||
| chr11:75351621-75351904 | Common:3; Rare:82 | ||||
| chr11:75399379-75399638 | Common:5; Rare:109 | ||||
| chr11:75399750-75400017 | Common:1; Rare:50 | ||||
| chr11:75400299-75400403 | Common:1; Rare:29 | ||||
| chr11:75429976-75430120 | Rare:42 | ||||
| chr11:75430147-75430325 | Common:1; Rare:76 | ||||
| chr11:75525821-75526201 | Common:2; Rare:114 | ||||
| chr11:75561978-75562148 | Rare:34; Clinvar:1; Clinvar (benign):1 |