| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:37221292-37221451 | Common:2; Rare:75 | ||||
| chr21:38907289-38907475 | Rare:37 | ||||
| chr21:44958875-44959189 | Common:5; Rare:68 | ||||
| chr21:44989555-44989785 | Common:5; Rare:47 | ||||
| chr21:44991813-44992114 | Common:7; Rare:56 | ||||
| chr21:45041338-45041607 | Common:3; Rare:52 | ||||
| chr21:45989494-45989652 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):3 | ||||
| chr22:16601175-16601482 | Common:2; Rare:123 | ||||
| chr22:17578268-17578465 | Rare:25 | ||||
| chr22:18068506-18068603 | Common:2; Rare:14 | ||||
| chr22:22298047-22298216 | Common:2; Rare:72 | ||||
| chr22:22306959-22307007 | Common:1; Rare:9 | ||||
| chr22:23181718-23181824 | Common:1; Rare:43 | ||||
| chr22:26672650-26672959 | Common:2; Rare:77 | ||||
| chr22:28796125-28796308 | Rare:45 |