| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:47037291-47037722 | Common:2; Rare:94 | ||||
| chr22:49657417-49657678 | Common:2; Rare:96 | ||||
| chr22:50191522-50191693 | Common:2; Rare:36 | ||||
| chr22:50314512-50314605 | Common:1; Rare:43 | ||||
| chr22:50526977-50527214 | Common:1; Rare:84; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:50539699-50539916 | Common:3; Rare:38 | ||||
| chr22:50548677-50548778 | Common:1; Rare:37 | ||||
| chr3:4977140-4977416 | Rare:51 | ||||
| chr3:4986903-4987056 | Rare:36 | ||||
| chr3:5199434-5199588 | Common:3; Rare:30 | ||||
| chr3:9390279-9390516 | Rare:60 | ||||
| chr3:9453809-9454029 | Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:9684962-9685232 | Rare:73 | ||||
| chr3:10193092-10193283 | Rare:40 | ||||
| chr3:11289176-11289395 | Common:1; Rare:44 |