| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40178428-40178557 | Rare:29 | ||||
| chr22:40346365-40346563 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40346862-40347012 | Common:3; Rare:38 | ||||
| chr22:40370436-40370673 | Rare:90 | ||||
| chr22:40636658-40637056 | Common:2; Rare:108 | ||||
| chr22:40679206-40679356 | Common:2; Rare:39 | ||||
| chr22:40818702-40819102 | Common:1; Rare:95 | ||||
| chr22:40819274-40819559 | Common:11; Rare:126 | ||||
| chr22:40856605-40856724 | Rare:49 | ||||
| chr22:40856914-40857170 | Common:2; Rare:104; Clinvar:4 | ||||
| chr22:40951060-40951410 | Common:2; Rare:123 | ||||
| chr22:40951608-40951995 | Common:3; Rare:107 | ||||
| chr22:41091379-41091891 | Common:7; Rare:187 | ||||
| chr22:41092075-41092420 | Common:3; Rare:187 | ||||
| chr22:41205122-41205397 | Common:2; Rare:88 |