| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45317508-45317779 | Common:2; Rare:58 | ||||
| chr21:45319708-45319844 | Common:1; Rare:28 | ||||
| chr22:19882135-19882157 | Rare:4 | ||||
| chr22:19886990-19887281 | Common:3; Rare:47 | ||||
| chr22:22298061-22298196 | Common:2; Rare:50 | ||||
| chr22:30969080-30969302 | Common:2; Rare:65 | ||||
| chr22:36288783-36289135 | Common:2; Rare:98; Clinvar:2; Clinvar (benign):4 | ||||
| chr22:38176171-38176396 | Common:1; Rare:48 | ||||
| chr22:46069073-46069236 | Rare:21 | ||||
| chr22:46069860-46070060 | Rare:43 | ||||
| chr22:46080067-46080372 | Common:1; Rare:96 | ||||
| chr3:14810480-14810770 | Common:2; Rare:103 | ||||
| chr3:39757371-39757513 | Common:1; Rare:19 | ||||
| chr3:43418645-43418802 | Rare:17 | ||||
| chr3:43496743-43496994 | Common:1; Rare:40 |