| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:11344589-11344718 | Rare:52 | ||||
| chr2:11344939-11345079 | Common:2; Rare:47 | ||||
| chr2:11465475-11465706 | Common:2; Rare:79 | ||||
| chr2:11465807-11466184 | Common:3; Rare:125 | ||||
| chr2:17753626-17754219 | Common:6; Rare:181; Clinvar (benign):1 | ||||
| chr2:18560635-18560800 | Rare:49 | ||||
| chr2:19901634-19901762 | Common:1; Rare:69 | ||||
| chr2:19901906-19902049 | Common:1; Rare:43 | ||||
| chr2:19975434-19975653 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:19990058-19990220 | Rare:40 | ||||
| chr2:20051528-20051832 | Common:1; Rare:86 | ||||
| chr2:20225345-20225559 | Common:1; Rare:59 | ||||
| chr2:20350316-20350430 | Common:1; Rare:41 | ||||
| chr2:20651044-20651194 | Rare:46 | ||||
| chr2:20823052-20823196 | Common:1; Rare:52 |